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873-31-4,MFCD00269951
Catalog No.:AA0032NT

873-31-4 | 1-Chloro-2-ethynylbenzene

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
96%
in stock  
$15.00   $10.00
- +
5g
97%
in stock  
$35.00   $25.00
- +
10g
96%
in stock  
$68.00   $47.00
- +
25g
96%
in stock  
$167.00   $117.00
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0032NT
Chemical Name:
1-Chloro-2-ethynylbenzene
CAS Number:
873-31-4
Molecular Formula:
C8H5Cl
Molecular Weight:
136.5783
MDL Number:
MFCD00269951
SMILES:
C#Cc1ccccc1Cl
Properties
Properties
 
BP:
82°C at 760 mmHg  
Form:
Liquid  
Refractive Index:
n20/D 1.5710(lit.)  
Solubility:
Soluble in hexane.  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
131  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
9  
Rotatable Bond Count:
1  
XLogP3:
2.8  

Upstream Synthesis Route

[1]GreenChemistry,2017,vol.19,#8,p.1983-1989

[2]EuropeanJournalofOrganicChemistry,2017,vol.2017,#4,p.781-785

[1]Chemosphere,2001,vol.42,#5-7,p.439-447

[1]Chemosphere,2001,vol.42,#5-7,p.439-447

[1]SyntheticCommunications,1990,vol.20,#12,p.1889-1892

[2]TetrahedronLetters,2003,vol.44,#41,p.7611-7612

[3]Organicandbiomolecularchemistry,2003,vol.1,#3,p.498-506

[4]Patent:WO2007/88014,2007,A1,.Locationinpatent:Page/Pagecolumn32-33

[5]JournalofMedicinalChemistry,2010,vol.53,#2,p.699-714

[6]AdvancedSynthesisandCatalysis,2014,vol.356,#11-12,p.2671-2678

[7]OrganicLetters,2014,vol.16,#24,p.6302-6305

[8]OrganicLetters,2015,vol.17,#10,p.2522-2525

[1]Tetrahedron,2005,vol.61,#16,p.4043-4052

[2]ChemistryLetters,2005,vol.34,#1,p.28-29

[3]ChemistryofHeterocyclicCompounds,2016,vol.52,#3,p.192-195

[4]Khim.Geterotsikl.Soedin.,2016,vol.52,#3,p.192-195,4

Downstream Synthesis Route
873-31-4   
1-chloro-2-(iodoethynyl)benzene 

[1]OrganicandBiomolecularChemistry,2018,vol.16,p.1508-1518

[2]Synlett,2018,vol.29,p.2051-2055

[3]Patent:CN108658724,2018,A.Locationinpatent:Paragraph0030;0031;0032

[4]RSCAdvances,2020,vol.10,p.3946-3950

[5]SyntheticCommunications,2008,vol.38,p.225-231

[6]Synlett,2020,vol.31,p.1102-1106

[7]JournaloftheAmericanChemicalSociety,1934,vol.56,p.1207

[1]OrganicLetters,2009,vol.11,p.709-712

[2]ChemistryLetters,2015,vol.44,p.129-131

[3]GreenChemistry,2019,vol.21,p.2899-2904

[4]BulletinoftheChemicalSocietyofJapan,2016,vol.89,p.794-797

[5]Synthesis,2010,p.3461-3466

[6]RSCAdvances,2016,vol.6,p.28653-28657

[7]BulletinoftheKoreanChemicalSociety,2012,vol.33,p.1325-1328

[8]TetrahedronLetters,2013,vol.54,p.3953-3955

[9]TetrahedronLetters,2020,vol.61

[10]GreenChemistry,2010,vol.12,p.45-48

[11]ResearchonChemicalIntermediates,2014,vol.40,p.1337-1344

[12]ChineseJournalofChemistry,2013,vol.31,p.187-194

[13]GreenChemistry,2009,vol.11,p.269-274

[14]TetrahedronLetters,2019,vol.60,p.1179-1181

[15]ACSCatalysis,2016,vol.6,p.868-872

[16]AppliedOrganometallicChemistry,2016,vol.30,p.943-945

[17]OrganicandBiomolecularChemistry,2013,vol.11,p.7451-7454

[18]AppliedOrganometallicChemistry,2014,vol.28,p.631-634

[19]AppliedOrganometallicChemistry,2011,vol.25,p.395-399

[20]Tetrahedron,2010,vol.66,p.4029-4031

[21]Synlett,2001,p.108-110

[22]Synthesis,2013,vol.45,p.1373-1379

[23]JournalofCatalysis,2014,vol.315,p.6-14

[24]OrganicLetters,2019,vol.21,p.9487-9492

[25]NewJournalofChemistry,2020,vol.44,p.4426-4439

[1]Tetrahedron,2001,vol.57,p.8017-8028

[2]ChemicalCommunications,2004,p.514-515

[3]JournalofOrganometallicChemistry,2018,vol.860,p.98-105

[4]JournaloftheAmericanChemicalSociety,2006,vol.128,p.581-590

[5]JournaloftheAmericanChemicalSociety,2018,vol.140,p.17666-17673

[1]InorganicChemistryCommunications,2019,vol.109

[2]Chemistry-AEuropeanJournal,2012,vol.18,p.11107-11114

[3]JournaloftheIranianChemicalSociety,2016,vol.13,p.1367-1374

[4]JournalofOrganometallicChemistry,2017,vol.851,p.46-51

[5]TetrahedronLetters,2013,vol.54,p.4414-4417

[6]AdvancedSynthesisandCatalysis,2016,vol.358,p.1433-1439

[7]JournalofOrganometallicChemistry,2015,vol.799-800,p.122-127

[8]JournalofOrganometallicChemistry,2019,vol.901

[9]CatalysisCommunications,2018,vol.115,p.78-81

[10]TetrahedronLetters,2018,vol.59,p.2075-2078

[11]EuropeanJournalofInorganicChemistry,2020,vol.2020,p.1000-1003

[12]AngewandteChemie-InternationalEdition,2002,vol.41,p.4563-4565

[13]Patent:US2005/143597,2005,A1.Locationinpatent:Page/Pagecolumn7

[14]OrganicSyntheses,2006,vol.83,p.55-60

[15]RSCAdvances,2018,vol.8,p.14829-14832

[16]Patent:CN109384677,2019,A.Locationinpatent:Paragraph0094-0097

[1]Patent:WO2007/88014,2007,A1.Locationinpatent:Page/Pagecolumn34-35

Literature

Title: Synthesis and excited-state photodynamics of a chlorin-bacteriochlorin dyad--through-space versus through-bond energy transfer in tetrapyrrole arrays.

Journal: Photochemistry and photobiology 20080101

Title: Photoinduced electron-transfer reactions of platinum(II) terpyridyl acetylide complexes: reductive quenching in a hydrogen-generating system.

Journal: Inorganic chemistry 20060529

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