3196-15-4
- Product Name：2-Bromobutyric acid methyl
- Molecular Formula：C5H9BrO2
- Purity：99%
- Molecular Weight：181.029
Product Details
pd_meltingpoint:116 °C
Appearance:clear slightly yellow liquid
Purity:99%
High quality purity >99% 2-Bromobutyric acid methyl 3196-15-4 for sale
- Molecular Formula:C5H9BrO2
- Molecular Weight:181.029
- Appearance/Colour:clear slightly yellow liquid
- Vapor Pressure:1.43mmHg at 25°C
- Melting Point:116 °C
- Refractive Index:n20/D 1.452(lit.)
- Boiling Point:171 °C at 760 mmHg
- Flash Point:58.4 °C
- PSA：26.30000
- Density:1.413 g/cm3
- LogP:1.33290
2-Bromobutyric acid methyl ester(Cas 3196-15-4) Usage
InChI:InChI=1/C5H9BrO2/c1-3-4(6)5(7)8-2/h4H,3H2,1-2H3/t4-/m1/s1
3196-15-4 Relevant articles
Cobalt-bisoxazoline-catalyzed asymmetric kumada cross-coupling of racemic α-bromo esters with aryl grignard reagents
Mao, Jianyou,Liu, Feipeng,Wang, Min,Wu, Lin,Zheng, Bing,Liu, Shangzhong,Zhong, Jiangchun,Bian, Qinghua,Walsh, Patrick J.
supporting information, p. 17662 - 17668 (2015/02/02)
The first cobalt-catalyzed asymmetric Ku...
GC separation of enantiomers of alkyl esters of 2-bromo substituted carboxylic acids enantiomers on 6-tbdms-2,3-di-alkyl- β- And γ-cyclodextrin stationary phases
Spanik, Ivan,Kaceriakova, Darina,Krupcik, Jan,Armstrong, Daniel Wayne
, p. 279 - 285 (2014/06/09)
The gas chromatographic separation of en...
Enoate reductase-mediated preparation of methyl (S)-2-bromobutanoate, a useful key intermediate for the synthesis of chiral active pharmaceutical ingredients
Brenna, Elisabetta,Gatti, Francesco G.,Manfredi, Alessia,Monti, Daniela,Parmeggiani, Fabio
experimental part, p. 262 - 268 (2012/06/18)
Enoate reductases belonging to the Old Y...
Enantioselectivity of haloalkane dehalogenases and its modulation by surface loop engineering
Prokop, Zbynek,Sato, Yukari,Brezovsky, Jan,Mozga, Tomas,Chaloupkova, Radka,Koudelakova, Tana,Jerabek, Petr,Stepankova, Veronika,Natsume, Ryo,Van Leeuwen, Jan G. E.,Janssen, Dick B.,Florian, Jan,Nagata, Yuji,Senda, Toshiya,Damborsky, Jiri
supporting information; experimental part, p. 6111 - 6115 (2010/11/05)
In the loop: Engineering of the surface ...
3196-15-4 Process route
-
-
67-56-1
methanol
-
-
80-58-0
2-Bromobutyric acid
-
-
3196-15-4,69043-96-5
Methyl 2-bromobutyrate
| Conditions | Yield |
|---|---|
|
With
dmap; dicyclohexyl-carbodiimide;
In
diethyl ether;
at 25 ℃;
for 3h;
Inert atmosphere;
|
69% |
-
-
141-75-3
butyryl chloride
-
-
3196-15-4,69043-96-5
Methyl 2-bromobutyrate
| Conditions | Yield |
|---|---|
|
With
bromine;
Erwaermen des Reaktionsprodukts mit Methanol;
|
3196-15-4 Upstream products
-
141-75-3
butyryl chloride
-
67-56-1
methanol
-
107-92-6
butyric acid
-
22118-12-3
2-bromobutanoyl chloride
3196-15-4 Downstream products
-
68039-27-0
methyl 2-ethyl-3-oxohexanoate
-
90794-35-7
2-(2-iodo-phenoxy)-butyric acid
-
90794-36-8
2-(4-iodo-phenoxy)-butyric acid
-
90888-05-4
2-(3-Iod-phenoxy)-buttersaeure
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