598-21-0
- Product Name：Bromoacetyl bromide
- Molecular Formula：C2H2Br2O
- Purity：99%
- Molecular Weight：201.845
Product Details
pd_meltingpoint:148.5°C (estimate)
Appearance:COA
Purity:99%
Buy high quality and low price Bromoacetyl bromide 598-21-0 now
- Molecular Formula:C2H2Br2O
- Molecular Weight:201.845
- Appearance/Colour:COA
- Vapor Pressure:3.8 mm Hg ( 25 °C)
- Melting Point:148.5°C (estimate)
- Refractive Index:n20/D 1.547(lit.)
- Boiling Point:148.5 °C at 760 mmHg
- Flash Point:72 °C
- PSA：17.07000
- Density:2.373 g/cm3
- LogP:1.30280
Bromoacetyl bromide(Cas 598-21-0) Usage
|
Air & Water Reactions |
Fumes in air. Reacts violently with water to form hydrobromic acid (HBr) (USCG 1991). |
|
Reactivity Profile |
Bromoacetyl bromide is incompatible with water, with bases (including amines), with strong oxidizing agents, with alcohols. May react vigorously or explosively if mixed with diisopropyl ether or other ethers in the presence of trace amounts of metal salts [J. Haz. Mat., 1981, 4, 291]. Decomposes when heated with evolution of highly toxic and irritating hydrogen bromide and bromophosgene vapors. |
|
Health Hazard |
Inhalation causes severe irritation of upper respiratory system. External contact causes severe irritation of eyes and skin. Ingestion causes severe irritation of mouth and stomach. |
|
General Description |
A water-white liquid with a pungent odor. Denser than water. Irritates skin, eyes and mucous membranes. May be toxic by ingestion, inhalation and skin absorption. Used to make other chemicals. |
InChI:InChI=1/C2H2Br2O/c3-1-2(4)5/h1H2
598-21-0 Relevant articles
Highly selective synthesis of α-bromoesters using molecular bromine catalyzed by phosphorus
Sun, Zhaoyun,Peng, Xinhua,Dong, Xiongzi,Shi, Wenwen
scheme or table, p. 929 - 930 (2012/07/30)
A series of α-bromoesters have been synt...
A matrix isolation study of the photochemically induced reactions of nitrogen dioxide with 1,2-dibromoethene and 1,2-dichloroethene using Fourier transform infrared spectroscopy
Clark, Robin J.H.,Foley, Loraine J.
, p. 1389 - 1393 (2007/10/03)
Photolyses of matrices of either BrCHCHB...
Method of synthesizing optically enriched alpha-halo-esters, and product and composition therefrom
-
, (2008/06/13)
A method of synthesizing highly opticall...
Specific isotope enrichment of methyl methacrylate
Werkhoven, Thekla M.,Van Nispen, Reinier,Lugtenburg, Johan
, p. 2909 - 2914 (2007/10/03)
A synthetic scheme has been developed to...
598-21-0 Process route
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-
7726-95-6
bromine
-
-
64-19-7,77671-22-8
acetic acid
-
-
506-96-7
Acetyl bromide
-
-
79-08-3
bromoacetic acid
-
-
598-21-0
2-Bromoacetyl bromide
| Conditions | Yield |
|---|---|
|
|
-
-
64-19-7,77671-22-8
acetic acid
-
-
598-21-0
2-Bromoacetyl bromide
| Conditions | Yield |
|---|---|
|
With
phosphorus; bromine; acetic anhydride;
|
|
|
With
phosphorus; bromine;
|
|
|
With
bromine; phosphorus tribromide;
at 20 - 75 ℃;
|
|
|
With
phosphorus; bromine; sodium hydroxide;
at 110 ℃;
regioselective reaction;
|
598-21-0 Upstream products
-
506-96-7
Acetyl bromide
-
593-92-0
vinylidene dibromide
-
64-19-7
acetic acid
-
79-08-3
bromoacetic acid
598-21-0 Downstream products
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13891-62-8
2-bromoethyl 2-bromoacetate
-
15109-94-1
1-(2-furyl)-2-bromoethanone
-
73326-20-2
2-bromo-N-(thiazol-2-yl)acetamide
-
66642-53-3
N-(pyridin-2-yl)-2-bromoacetamide
Relevant Products
-
4-Bromobenzoic acidCAS：586-76-5
-
1,2-DibromoethaneCAS：106-93-4
-
2-BromoanthraquinoneCAS：572-83-8
