Basic information Safety Supplier Related

[1-(Ethoxycarbonyl)ethyl]triphenylphosphonium bromide

Basic information Safety Supplier Related

[1-(Ethoxycarbonyl)ethyl]triphenylphosphonium bromide Basic information

Product Name:
[1-(Ethoxycarbonyl)ethyl]triphenylphosphonium bromide
Synonyms:
  • [1-(ETHOXYCARBONYL)ETHYL]TRIPHENYL PHOSPHONIUM BROMIDE, 95+%
  • (1-ETHOXYCARBONYLETHYL)TRIPHENYLPHOSPHONIUM BROMIDE
  • 1-CARBETHOXYETHYL TRIPHENYLPHOSPHONIUM BROMIDE
  • (2-ethoxy-1-methyl-2-oxoethyl)triphenylphosphonium bromide
  • carbethoxy Ethyl Triphenyl Phosphonium Bromide
  • (1-ETHOXYCARBONYLETHYL)TRIPHENYLPHOSPHONIUM BROMIDE 96%
  • 1-Carbethoxyethyl triphenylphosphonium bromide 98%
  • (1-carboethoxyethyl)triphenylphosphonium bromide
CAS:
30018-16-7
MF:
C23H24BrO2P
MW:
443.32
EINECS:
250-002-2
Product Categories:
  • Isoquinolines ,Quinolines ,Quinazolines ,Quinaldines
Mol File:
30018-16-7.mol
More
Less

[1-(Ethoxycarbonyl)ethyl]triphenylphosphonium bromide Chemical Properties

Melting point:
152 °C
storage temp. 
Refrigerator (+4°C)
solubility 
Chloroform, Methanol
form 
Solid
color 
Pale Yellow
Water Solubility 
soluble
Sensitive 
Hygroscopic
BRN 
3822244
InChI
InChI=1S/C23H24O2P.BrH/c1-3-25-23(24)19(2)26(20-13-7-4-8-14-20,21-15-9-5-10-16-21)22-17-11-6-12-18-22;/h4-19H,3H2,1-2H3;1H/q+1;/p-1
InChIKey
RSYXORMKBUFAMS-UHFFFAOYSA-M
SMILES
[P+](C1C=CC=CC=1)(C1C=CC=CC=1)(C1C=CC=CC=1)C(C)C(=O)OCC.[Br-]
CAS DataBase Reference
30018-16-7(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-29-22
Safety Statements 
26-36-8-37/39
Hazard Note 
Irritant/Hygroscopic
HS Code 
29310099

MSDS

  • Language:English Provider:ALFA
More
Less

[1-(Ethoxycarbonyl)ethyl]triphenylphosphonium bromide Usage And Synthesis

Chemical Properties

White to off-white powder

Uses

suzuki reaction

Uses

1-Ethoxycarbonylethyl)triphenylphosphonium bromide is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. It is widely used as an organophosphine catalyst.

Synthesis

603-35-0

535-11-5

30018-16-7

1.0 g of triphenylphosphine was dissolved in 15 mL of ethyl acetate and 0.55 mL of ethyl 2-bromopropionate was added to this solution. The reaction mixture was stirred at room temperature for 24 hours. Upon completion of the reaction, the bulk of the resulting white solid product was collected by diafiltration. The solids were washed with ethyl acetate to give a final 1.35 g of white solid product ethoxycarbonyl ethyltriphenylphosphonium bromide in 80.5% yield.

References

[1] European Journal of Organic Chemistry, 2016, vol. 2016, # 12, p. 2110 - 2114
[2] Chemistry - A European Journal, 2015, vol. 21, # 20, p. 7408 - 7412
[3] Tetrahedron, 2010, vol. 66, # 26, p. 4745 - 4759
[4] Journal of Organic Chemistry, 1984, vol. 49, # 22, p. 4293 - 4295
[5] Patent: CN103864753, 2016, B. Location in patent: Paragraph 0087; 0110-0111

[1-(Ethoxycarbonyl)ethyl]triphenylphosphonium bromideSupplier

Creasyn Finechem(Tianjin) Co., Ltd.
Tel
022-83946278 13820503911
Email
sales@creasyn.com
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
ShangHai DEMO Chemical Co.,Ltd
Tel
400-021-7337 2355568890
Email
sales@demochem.com
Beijing HwrkChemical Technology Co., Ltd
Tel
18515581800 18501085097
Email
sales.bj@hwrkchemical.com