+1 858-523-8231
Login | Register
menu
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
54314-84-0,MFCD00134570
Catalog No.:AA003O0W

54314-84-0 | Benzyl 3-bromopropyl ether

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
96%
in stock  
$8.00   $6.00
- +
5g
96%
in stock  
$14.00   $10.00
- +
10g
96%
in stock  
$17.00   $12.00
- +
25g
96%
in stock  
$37.00   $26.00
- +
100g
96%
in stock  
$146.00   $103.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003O0W
Chemical Name:
Benzyl 3-bromopropyl ether
CAS Number:
54314-84-0
Molecular Formula:
C10H13BrO
Molecular Weight:
229.1136
MDL Number:
MFCD00134570
SMILES:
BrCCCOCc1ccccc1
Properties
Properties
 
BP:
251.7±15.0°C at 760 mmHg  
Form:
Liquid  
Refractive Index:
n20/D 1.531(lit.)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
100  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
5  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
2.7  

Synonyms
 
  
Upstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,2008,vol.130,#18,p.6018-6024

[2]BeilsteinJournalofOrganicChemistry,2018,vol.14,p.2730-2736

[3]Patent:WO2008/157726,2008,A1,.Locationinpatent:Page/Pagecolumn220

[4]TetrahedronLetters,2016,vol.57,#13,p.1486-1488

[5]JournaloftheAmericanChemicalSociety,1982,vol.104,#4,p.1054-1068

[6]LiebigsAnnalenderChemie,1989,p.719-726

[7]ArchivderPharmazie,1995,vol.328,#1,p.45-52

[8]JournaloftheAmericanChemicalSociety,1943,vol.65,p.1280

[9]Chem.Abstr.,1947,p.5543

[10]Tetrahedron,1982,vol.38,#11,p.1647-1656

[11]JournaloftheAmericanChemicalSociety,1985,vol.107,#9,p.2730-2737

[12]TetrahedronLetters,1993,vol.34,#1,p.133-136

[13]JournalofOrganicChemistry,1993,vol.58,#6,p.1458-1465

[14]AngewandteChemie-InternationalEdition,2002,vol.41,#22,p.4316-4318

[15]CanadianJournalofChemistry,1996,vol.74,#12,p.2487-2502

[16]TetrahedronLetters,2014,vol.55,#52,p.7177-7180

[17]EuropeanJournalofOrganicChemistry,2015,vol.2015,#1,p.81-85

[1]Patent:US4066692,1978,A,

[1]AdvancedSynthesisandCatalysis,2008,vol.350,#7-8,p.1163-1167

[1]BeilsteinJournalofOrganicChemistry,2018,vol.14,p.2730-2736

[2]BeilsteinJournalofOrganicChemistry,2018,vol.14,p.2730-2736

[1]TetrahedronLetters,2002,vol.43,#50,p.9225-9227

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,2008,vol.130,p.6018-6024

[2]BeilsteinJournalofOrganicChemistry,2018,vol.14,p.2730-2736

[3]Patent:WO2008/157726,2008,A1.Locationinpatent:Page/Pagecolumn220

[4]TetrahedronLetters,2016,vol.57,p.1486-1488

[5]JournaloftheAmericanChemicalSociety,1982,vol.104,p.1054-1068

[6]OrganicandBiomolecularChemistry,2019,vol.17,p.1744-1748

[7]LiebigsAnnalenderChemie,1989,p.719-726

[8]ArchivderPharmazie,1995,vol.328,p.45-52

[9]JournaloftheAmericanChemicalSociety,1943,vol.65,p.1280    Chem.Abstr.,1947,p.5543

[10]Tetrahedron,1982,vol.38,p.1647-1656

[11]JournaloftheAmericanChemicalSociety,1985,vol.107,p.2730-2737

[12]TetrahedronLetters,1993,vol.34,p.133-136

[13]JournalofOrganicChemistry,1993,vol.58,p.1458-1465

[14]AngewandteChemie-InternationalEdition,2002,vol.41,p.4316-4318

[15]CanadianJournalofChemistry,1996,vol.74,p.2487-2502

[16]TetrahedronLetters,2014,vol.55,p.7177-7180

[17]EuropeanJournalofOrganicChemistry,2015,vol.2015,p.81-85

[1]JournaloftheAmericanChemicalSociety,1985,vol.107,p.2730-2737

[2]JournalofOrganicChemistry,1984,vol.49,p.2326-2332

[3]JournalofOrganicChemistry,1994,vol.59,p.8092-8100

[4]BulletinoftheChemicalSocietyofJapan,1978,vol.51,p.265-270

[5]Patent:DE2354085,1974,    Chem.Abstr.,1974,vol.81

[1]JournaloftheAmericanChemicalSociety,2009,vol.131,p.2786-2787

[2]LiebigsAnnalenderChemie,1989,p.719-726

[3]Patent:WO2014/136086,2014,A1.Locationinpatent:Page/Pagecolumn158

[1]TetrahedronLetters,2002,vol.43,p.1205-1208

[1]JournaloftheAmericanChemicalSociety,2008,vol.130,p.6018-6024

[2]AngewandteChemie-InternationalEdition,2002,vol.41,p.4316-4318

Literature
Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
Submit
SDS
Related Products of 54314-84-0
148173-18-6

148173-18-6

 1443110-01-7

1443110-01-7

 1807941-88-3

1807941-88-3

 179993-02-3

179993-02-3

 90841-55-7

90841-55-7
Building Blocks
More >
Tags:54314-84-0 Molecular Formula|54314-84-0 MDL|54314-84-0 SMILES|54314-84-0 Benzyl 3-bromopropyl ether
Catalog No.: AA003O0W
54314-84-0,MFCD00134570
54314-84-0 | Benzyl 3-bromopropyl ether
Pack Size： 1g
Purity： 96%
in stock
$8.00 $6.00
Pack Size： 5g
Purity： 96%
in stock
$14.00 $10.00
Pack Size： 10g
Purity： 96%
in stock
$17.00 $12.00
Pack Size： 25g
Purity： 96%
in stock
$37.00 $26.00
Pack Size： 100g
Purity： 96%
in stock
$146.00 $103.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003O0W
Chemical Name: Benzyl 3-bromopropyl ether
CAS Number: 54314-84-0
Molecular Formula: C10H13BrO
Molecular Weight: 229.1136
MDL Number: MFCD00134570
SMILES: BrCCCOCc1ccccc1
Properties
BP: 251.7±15.0°C at 760 mmHg  
Form: Liquid  
Refractive Index: n20/D 1.531(lit.)  
Storage: Inert atmosphere;Room Temperature;  
Complexity: 100  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 5  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 2.7  
68:   
Upstream Synthesis Route
4799-68-2    54314-84-0 

[1]JournaloftheAmericanChemicalSociety,2008,vol.130,#18,p.6018-6024

[2]BeilsteinJournalofOrganicChemistry,2018,vol.14,p.2730-2736

[3]Patent:WO2008/157726,2008,A1,.Locationinpatent:Page/Pagecolumn220

[4]TetrahedronLetters,2016,vol.57,#13,p.1486-1488

[5]JournaloftheAmericanChemicalSociety,1982,vol.104,#4,p.1054-1068

[6]LiebigsAnnalenderChemie,1989,p.719-726

[7]ArchivderPharmazie,1995,vol.328,#1,p.45-52

[8]JournaloftheAmericanChemicalSociety,1943,vol.65,p.1280

[9]Chem.Abstr.,1947,p.5543

[10]Tetrahedron,1982,vol.38,#11,p.1647-1656

[11]JournaloftheAmericanChemicalSociety,1985,vol.107,#9,p.2730-2737

[12]TetrahedronLetters,1993,vol.34,#1,p.133-136

[13]JournalofOrganicChemistry,1993,vol.58,#6,p.1458-1465

[14]AngewandteChemie-InternationalEdition,2002,vol.41,#22,p.4316-4318

[15]CanadianJournalofChemistry,1996,vol.74,#12,p.2487-2502

[16]TetrahedronLetters,2014,vol.55,#52,p.7177-7180

[17]EuropeanJournalofOrganicChemistry,2015,vol.2015,#1,p.81-85

108-86-1    54314-83-9    54314-84-0 

[1]Patent:US4066692,1978,A,

14593-43-2    54314-84-0 

[1]AdvancedSynthesisandCatalysis,2008,vol.350,#7-8,p.1163-1167

4799-68-2    68-12-2    54314-84-0 

[1]BeilsteinJournalofOrganicChemistry,2018,vol.14,p.2730-2736

[2]BeilsteinJournalofOrganicChemistry,2018,vol.14,p.2730-2736

100-52-7    54314-84-0    92411-30-8 

[1]TetrahedronLetters,2002,vol.43,#50,p.9225-9227

Downstream Synthesis Route
4799-68-2    54314-84-0 

[1]JournaloftheAmericanChemicalSociety,2008,vol.130,p.6018-6024

[2]BeilsteinJournalofOrganicChemistry,2018,vol.14,p.2730-2736

[3]Patent:WO2008/157726,2008,A1.Locationinpatent:Page/Pagecolumn220

[4]TetrahedronLetters,2016,vol.57,p.1486-1488

[5]JournaloftheAmericanChemicalSociety,1982,vol.104,p.1054-1068

[6]OrganicandBiomolecularChemistry,2019,vol.17,p.1744-1748

[7]LiebigsAnnalenderChemie,1989,p.719-726

[8]ArchivderPharmazie,1995,vol.328,p.45-52

[9]JournaloftheAmericanChemicalSociety,1943,vol.65,p.1280    Chem.Abstr.,1947,p.5543

[10]Tetrahedron,1982,vol.38,p.1647-1656

[11]JournaloftheAmericanChemicalSociety,1985,vol.107,p.2730-2737

[12]TetrahedronLetters,1993,vol.34,p.133-136

[13]JournalofOrganicChemistry,1993,vol.58,p.1458-1465

[14]AngewandteChemie-InternationalEdition,2002,vol.41,p.4316-4318

[15]CanadianJournalofChemistry,1996,vol.74,p.2487-2502

[16]TetrahedronLetters,2014,vol.55,p.7177-7180

[17]EuropeanJournalofOrganicChemistry,2015,vol.2015,p.81-85

54314-84-0    603-35-0    54314-85-1 

[1]JournaloftheAmericanChemicalSociety,1985,vol.107,p.2730-2737

[2]JournalofOrganicChemistry,1984,vol.49,p.2326-2332

[3]JournalofOrganicChemistry,1994,vol.59,p.8092-8100

[4]BulletinoftheChemicalSocietyofJapan,1978,vol.51,p.265-270

[5]Patent:DE2354085,1974,    Chem.Abstr.,1974,vol.81

54314-84-0    105-53-3    82258-55-7 

[1]JournaloftheAmericanChemicalSociety,2009,vol.131,p.2786-2787

[2]LiebigsAnnalenderChemie,1989,p.719-726

[3]Patent:WO2014/136086,2014,A1.Locationinpatent:Page/Pagecolumn158

54314-84-0    17288-40-3    438468-78-1 

[1]TetrahedronLetters,2002,vol.43,p.1205-1208

54314-84-0    86-93-1    1023306-27-5 

[1]JournaloftheAmericanChemicalSociety,2008,vol.130,p.6018-6024

[2]AngewandteChemie-InternationalEdition,2002,vol.41,p.4316-4318

Related Products of of 54314-84-0
148173-18-6
148173-18-6
1443110-01-7
1443110-01-7
1807941-88-3
1807941-88-3
179993-02-3
179993-02-3
90841-55-7
90841-55-7
Building Blocks More >
333-36-8
333-36-8
Bis(2,2,2-trifluoroethyl) ether
AA003O4U | MFCD00010604
18457-04-0
18457-04-0
Bis(trimethylsilyl) malonate
AA003O9V | MFCD00009631
18942-49-9
18942-49-9
Boc-D-Phe-OH
AA003ODZ | MFCD00063149
15481-39-7
15481-39-7
BROMINE-1,4-DIOXANE COMPLEX
AA003OH6 | MFCD00034818
50292-00-7
50292-00-7
Caprylohydroxamic acid sodium salt
AA003OM7 | MFCD00058968
40244-90-4
40244-90-4
Chlorodiisopropylphosphine
AA003OQS | MFCD00015027
73094-35-6
73094-35-6
Cis-4-(hydroxymethyl)cyclohexanecarboxylic acid
AA003OW6 | MFCD10566906
26426-65-3
26426-65-3
CYCLOHEPTENE
AA003P1K | MFCD00004156
24277-44-9
24277-44-9
D-ALPHA-METHYLBENZYL ISOTHIOCYANATE
AA003P5J | MFCD00135478
2155-60-4
2155-60-4
Dibutyl 2-methylenesuccinate
AA003P9H | MFCD00027211
Submit
© 2017 AA BLOCKS, INC. All rights reserved.