29176-55-4,MFCD02084186
Catalog No.:AA002XHV

29176-55-4 | 2,9-Dichloro-1,10-phenanthroline

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
95%
in stock  
$6.00   $4.00
- +
250mg
98%
in stock  
$9.00   $6.00
- +
1g
98%
in stock  
$28.00   $19.00
- +
5g
98%
in stock  
$96.00   $67.00
- +
10g
95%
in stock  
$144.00   $101.00
- +
25g
95%
in stock  
$358.00   $251.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA002XHV
Chemical Name:
2,9-Dichloro-1,10-phenanthroline
CAS Number:
29176-55-4
Molecular Formula:
C12H6Cl2N2
Molecular Weight:
249.0954
MDL Number:
MFCD02084186
SMILES:
Clc1ccc2c(n1)c1nc(Cl)ccc1cc2
NSC Number:
608430
Properties
Properties
 
Form:
Solid  
MP:
249-250℃  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
235  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
4.4  

Upstream Synthesis Route

[1]BeilsteinJournalofOrganicChemistry,2014,vol.10,p.814-824

[2]EuropeanJournalofInorganicChemistry,2017,vol.2017,#34,p.4020-4027

[3]Chemistry-AEuropeanJournal,2007,vol.13,#27,p.7584-7594

[4]Organometallics,2013,vol.32,#21,p.6511-6521

[5]Chemistry-AEuropeanJournal,2014,vol.20,#25,p.7819-7829

[6]Patent:US9074266,2015,B2,.Locationinpatent:Page/Pagecolumn8

[7]OrganicPreparationsandProceduresInternational,2012,vol.44,#4,p.392-396

[8]Chemistry-AEuropeanJournal,2015,vol.21,#23,p.8426-8434

[9]RSCAdvances,2016,vol.6,#46,p.39663-39674

[10]DaltonTransactions,2017,vol.46,#7,p.2238-2248

[11]InorganicChemistry,2018,vol.57,#21,p.13461-13469

[12]Chemistry-AEuropeanJournal,2016,vol.22,#42,p.14881-14889

[13]JournalofOrganicChemistry,2010,vol.75,#20,p.6858-6868

[14]BulletinoftheChemicalSocietyofJapan,1990,vol.63,#9,p.2710-2712

[15]Chemistry-AnAsianJournal,2013,vol.8,#7,p.1368-1371

[16]EuropeanJournalofOrganicChemistry,2009,#14,p.2328-2341

[1]Patent:WO2011/30566,2011,A1,.Locationinpatent:Page/Pagecolumn24-25

[2]Patent:WO2012/124310,2012,A1,.Locationinpatent:Page/Pagecolumn35

[3]TetrahedronLetters,1989,vol.30,#4,p.463-466

[4]JournaloftheIndianChemicalSociety,1993,vol.70,#11-12,p.877-884

[5]JournalofOrganicChemistry,2000,vol.65,#23,p.7757-7763

[6]OrganicPreparationsandProceduresInternational,2007,vol.39,#6,p.603-608

[1]JournaloftheChemicalSociety,DaltonTransactions:InorganicChemistry(1972-1999),1980,p.736-742

[2]JournaloftheIndianChemicalSociety,1993,vol.70,#11-12,p.877-884

[3]EuropeanJournalofOrganicChemistry,2009,#14,p.2328-2341

[4]Patent:WO2011/30566,2011,A1,

[5]Patent:WO2012/124310,2012,A1,

[1]JournaloftheIndianChemicalSociety,1993,vol.70,#11-12,p.877-884

[2]BulletinoftheChemicalSocietyofJapan,1990,vol.63,#9,p.2710-2712

[3]Patent:WO2011/30566,2011,A1,

[4]OrganicPreparationsandProceduresInternational,2012,vol.44,#4,p.392-396

[5]Patent:WO2012/124310,2012,A1,

[6]Chemistry-AnAsianJournal,2013,vol.8,#7,p.1368-1371

[7]Organometallics,2013,vol.32,#21,p.6511-6521

[8]BeilsteinJournalofOrganicChemistry,2014,vol.10,p.814-824

[9]Chemistry-AEuropeanJournal,2014,vol.20,#25,p.7819-7829

[10]Patent:US9074266,2015,B2,

[11]Chemistry-AEuropeanJournal,2015,vol.21,#23,p.8426-8434

[12]RSCAdvances,2016,vol.6,#46,p.39663-39674

[13]Chemistry-AEuropeanJournal,2016,vol.22,#42,p.14881-14889

[14]DaltonTransactions,2017,vol.46,#7,p.2238-2248

[15]EuropeanJournalofInorganicChemistry,2017,vol.2017,#34,p.4020-4027

[16]InorganicChemistry,2018,vol.57,#21,p.13461-13469

[1]Chemistry-AnAsianJournal,2013,vol.8,#7,p.1368-1371

[2]Organometallics,2013,vol.32,#21,p.6511-6521

[3]BeilsteinJournalofOrganicChemistry,2014,vol.10,p.814-824

[4]Chemistry-AEuropeanJournal,2014,vol.20,#25,p.7819-7829

[5]Patent:US9074266,2015,B2,

[6]Chemistry-AEuropeanJournal,2015,vol.21,#23,p.8426-8434

[7]RSCAdvances,2016,vol.6,#46,p.39663-39674

[8]Chemistry-AEuropeanJournal,2016,vol.22,#42,p.14881-14889

[9]EuropeanJournalofInorganicChemistry,2017,vol.2017,#34,p.4020-4027

[10]InorganicChemistry,2018,vol.57,#21,p.13461-13469

Downstream Synthesis Route

[1]JustusLiebigsAnnalenderChemie,1977,p.1080-1086

[1]JournaloftheChemicalSociety,DaltonTransactions,1980,p.736-742

[2]JournaloftheIndianChemicalSociety,1993,vol.70,p.877-884

[3]EuropeanJournalofOrganicChemistry,2009,p.2328-2341

[4]Patent:WO2011/30566,2011,A1

[5]Patent:WO2012/124310,2012,A1

[6]Patent:CN109776532,2019,A

[1]TetrahedronLetters,1996,vol.37,p.267-270

[1]Huber,FabianL.;Nauroozi,Djawed;Mengele,AlexanderK.;Rau,Sven[EuropeanJournalofInorganicChemistry,2017,vol.2017,#34,p.4020-4027]

[2]Zong,Ruifa;Thummel,RandolphP.[JournaloftheAmericanChemicalSociety,2004,vol.126,#35,p.10800-10801]

[1]Hamilton,CharlesW.;Laitar,DavidS.;Sadighi,JosephP.[ChemicalCommunications,2004,#14,p.1628-1629]

Literature

Title: (Butane-1,3-diyne-1,4-diyl)bis-(tri-isopropyl-silane).

Journal: Acta crystallographica. Section E, Structure reports online 20100801

Title: 2,9-Dichloro-1,10-phenanthroline.

Journal: Acta crystallographica. Section E, Structure reports online 20090401

Title: 2,2';9',2''-Ter[1,10]phenanthroline.

Journal: Inorganic chemistry 20050822

Title: 2,9-Di-(2'-pyridyl)-1,10-phenanthroline: a tetradentate ligand for Ru(II).

Journal: Journal of the American Chemical Society 20040908

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SDS
Historical Records
Tags:29176-55-4 Molecular Formula|29176-55-4 MDL|29176-55-4 SMILES|29176-55-4 2,9-Dichloro-1,10-phenanthroline
Catalog No.: AA002XHV
29176-55-4,MFCD02084186
29176-55-4 | 2,9-Dichloro-1,10-phenanthroline
Pack Size: 100mg
Purity: 95%
in stock
$6.00 $4.00
Pack Size: 250mg
Purity: 98%
in stock
$9.00 $6.00
Pack Size: 1g
Purity: 98%
in stock
$28.00 $19.00
Pack Size: 5g
Purity: 98%
in stock
$96.00 $67.00
Pack Size: 10g
Purity: 95%
in stock
$144.00 $101.00
Pack Size: 25g
Purity: 95%
in stock
$358.00 $251.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA002XHV
Chemical Name: 2,9-Dichloro-1,10-phenanthroline
CAS Number: 29176-55-4
Molecular Formula: C12H6Cl2N2
Molecular Weight: 249.0954
MDL Number: MFCD02084186
SMILES: Clc1ccc2c(n1)c1nc(Cl)ccc1cc2
NSC Number: 608430
Properties
Form: Solid  
MP: 249-250℃  
Storage: Inert atmosphere;2-8℃;  
Complexity: 235  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 4.4  
Upstream Synthesis Route
39588-59-5    29176-55-4 

[1]BeilsteinJournalofOrganicChemistry,2014,vol.10,p.814-824

[2]EuropeanJournalofInorganicChemistry,2017,vol.2017,#34,p.4020-4027

[3]Chemistry-AEuropeanJournal,2007,vol.13,#27,p.7584-7594

[4]Organometallics,2013,vol.32,#21,p.6511-6521

[5]Chemistry-AEuropeanJournal,2014,vol.20,#25,p.7819-7829

[6]Patent:US9074266,2015,B2,.Locationinpatent:Page/Pagecolumn8

[7]OrganicPreparationsandProceduresInternational,2012,vol.44,#4,p.392-396

[8]Chemistry-AEuropeanJournal,2015,vol.21,#23,p.8426-8434

[9]RSCAdvances,2016,vol.6,#46,p.39663-39674

[10]DaltonTransactions,2017,vol.46,#7,p.2238-2248

[11]InorganicChemistry,2018,vol.57,#21,p.13461-13469

[12]Chemistry-AEuropeanJournal,2016,vol.22,#42,p.14881-14889

[13]JournalofOrganicChemistry,2010,vol.75,#20,p.6858-6868

[14]BulletinoftheChemicalSocietyofJapan,1990,vol.63,#9,p.2710-2712

[15]Chemistry-AnAsianJournal,2013,vol.8,#7,p.1368-1371

[16]EuropeanJournalofOrganicChemistry,2009,#14,p.2328-2341

29176-54-3    29176-55-4 

[1]Patent:WO2011/30566,2011,A1,.Locationinpatent:Page/Pagecolumn24-25

[2]Patent:WO2012/124310,2012,A1,.Locationinpatent:Page/Pagecolumn35

[3]TetrahedronLetters,1989,vol.30,#4,p.463-466

[4]JournaloftheIndianChemicalSociety,1993,vol.70,#11-12,p.877-884

[5]JournalofOrganicChemistry,2000,vol.65,#23,p.7757-7763

[6]OrganicPreparationsandProceduresInternational,2007,vol.39,#6,p.603-608

7089-68-1    29176-55-4 

[1]JournaloftheChemicalSociety,DaltonTransactions:InorganicChemistry(1972-1999),1980,p.736-742

[2]JournaloftheIndianChemicalSociety,1993,vol.70,#11-12,p.877-884

[3]EuropeanJournalofOrganicChemistry,2009,#14,p.2328-2341

[4]Patent:WO2011/30566,2011,A1,

[5]Patent:WO2012/124310,2012,A1,

66-71-7    29176-55-4 

[1]JournaloftheIndianChemicalSociety,1993,vol.70,#11-12,p.877-884

[2]BulletinoftheChemicalSocietyofJapan,1990,vol.63,#9,p.2710-2712

[3]Patent:WO2011/30566,2011,A1,

[4]OrganicPreparationsandProceduresInternational,2012,vol.44,#4,p.392-396

[5]Patent:WO2012/124310,2012,A1,

[6]Chemistry-AnAsianJournal,2013,vol.8,#7,p.1368-1371

[7]Organometallics,2013,vol.32,#21,p.6511-6521

[8]BeilsteinJournalofOrganicChemistry,2014,vol.10,p.814-824

[9]Chemistry-AEuropeanJournal,2014,vol.20,#25,p.7819-7829

[10]Patent:US9074266,2015,B2,

[11]Chemistry-AEuropeanJournal,2015,vol.21,#23,p.8426-8434

[12]RSCAdvances,2016,vol.6,#46,p.39663-39674

[13]Chemistry-AEuropeanJournal,2016,vol.22,#42,p.14881-14889

[14]DaltonTransactions,2017,vol.46,#7,p.2238-2248

[15]EuropeanJournalofInorganicChemistry,2017,vol.2017,#34,p.4020-4027

[16]InorganicChemistry,2018,vol.57,#21,p.13461-13469

15302-99-5    29176-55-4 

[1]Chemistry-AnAsianJournal,2013,vol.8,#7,p.1368-1371

[2]Organometallics,2013,vol.32,#21,p.6511-6521

[3]BeilsteinJournalofOrganicChemistry,2014,vol.10,p.814-824

[4]Chemistry-AEuropeanJournal,2014,vol.20,#25,p.7819-7829

[5]Patent:US9074266,2015,B2,

[6]Chemistry-AEuropeanJournal,2015,vol.21,#23,p.8426-8434

[7]RSCAdvances,2016,vol.6,#46,p.39663-39674

[8]Chemistry-AEuropeanJournal,2016,vol.22,#42,p.14881-14889

[9]EuropeanJournalofInorganicChemistry,2017,vol.2017,#34,p.4020-4027

[10]InorganicChemistry,2018,vol.57,#21,p.13461-13469

Downstream Synthesis Route
1191-62-4    29176-55-4    64765-44-2 

[1]JustusLiebigsAnnalenderChemie,1977,p.1080-1086

7089-68-1    29176-55-4 

[1]JournaloftheChemicalSociety,DaltonTransactions,1980,p.736-742

[2]JournaloftheIndianChemicalSociety,1993,vol.70,p.877-884

[3]EuropeanJournalofOrganicChemistry,2009,p.2328-2341

[4]Patent:WO2011/30566,2011,A1

[5]Patent:WO2012/124310,2012,A1

[6]Patent:CN109776532,2019,A

126617-98-9    29176-55-4    126617-90-1 

[1]TetrahedronLetters,1996,vol.37,p.267-270

17997-47-6    29176-55-4    773883-32-2 

[1]Huber,FabianL.;Nauroozi,Djawed;Mengele,AlexanderK.;Rau,Sven[EuropeanJournalofInorganicChemistry,2017,vol.2017,#34,p.4020-4027]

[2]Zong,Ruifa;Thummel,RandolphP.[JournaloftheAmericanChemicalSociety,2004,vol.126,#35,p.10800-10801]

344-04-7    29176-55-4    757191-46-1 

[1]Hamilton,CharlesW.;Laitar,DavidS.;Sadighi,JosephP.[ChemicalCommunications,2004,#14,p.1628-1629]

Literature fold

Title: (Butane-1,3-diyne-1,4-diyl)bis-(tri-isopropyl-silane).

Journal: Acta crystallographica. Section E, Structure reports online20100801

Title: 2,9-Dichloro-1,10-phenanthroline.

Journal: Acta crystallographica. Section E, Structure reports online20090401

Title: 2,2';9',2''-Ter[1,10]phenanthroline.

Journal: Inorganic chemistry20050822

Title: 2,9-Di-(2'-pyridyl)-1,10-phenanthroline: a tetradentate ligand for Ru(II).

Journal: Journal of the American Chemical Society20040908

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