Name | 3-Bromo-2-(bromomethyl)propionic acid |
Synonyms | bis(bromomethyl)acetic acid β,β'-dibromoisobutyric acid BETA,BETA'-DIBROMOISOBUTYRIC ACID 3-bromo-2-(bromomethyl)propanoate 3-BROMO-2-(BROMOMETHYL)PROPANOIC ACID 3-Bromo-2-(bromomethyl)propionic acid 3-bromo-2-(bromomethyl)propanoic acid 3-BROMO-2-(BROMOMETHYL)PROPIONIC ACID Propanoic acid, 3-bromo-2-(bromomethyl)- 3-BROMO-2-(BROMOMETHYL)PROPIONIC ACID (KG LEVEL) |
CAS | 41459-42-1 |
InChI | InChI=1/C4H6Br2O2/c5-1-3(2-6)4(7)8/h3H,1-2H2,(H,7,8)/p-1 |
Molecular Formula | C4H6Br2O2 |
Molar Mass | 245.9 |
Density | 2.121±0.06 g/cm3(Predicted) |
Melting Point | 98-101°C(lit.) |
Boling Point | 286.7±30.0 °C(Predicted) |
Flash Point | 127.2°C |
Solubility | Soluble in acetic acid. |
Vapor Presure | 0.000666mmHg at 25°C |
Appearance | Crystalline Powder |
Color | Off-white to brown |
BRN | 1752505 |
pKa | 3.33±0.11(Predicted) |
Storage Condition | Inert atmosphere,2-8°C |
MDL | MFCD00010643 |
Hazard Symbols | C - Corrosive |
Risk Codes | 34 - Causes burns |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
UN IDs | UN 3261 8/PG 2 |
WGK Germany | 3 |
FLUKA BRAND F CODES | 8 |
HS Code | 29159000 |
Hazard Class | 8 |
Packing Group | III |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
Introduction | 3-bromo-2-bromomethylpropionic acid is an organic intermediate that can be made of bis (hydroxymethyl) malonate diethyl ester and hydrogen bromide Preparation by one-step reaction. There are reports that it can be used to prepare Erk inhibitors. |
Uses | 3-bromo-2-bromomethylpropionic acid is an organic intermediate, and it has been reported in the literature that it can be used to prepare Erk inhibitors. |
Preparation | Commercially available diethyl bis (hydroxymethyl) malonate (25g, 0.11 mol) and 48% The mixture of aqueous hydrogen bromide (192 cubic centimeters, 1.70 mol) is heated until the bromoethane liquid starts to evaporate from the mixture, and then vigorously distilled for about 1h. the reaction mixture was refluxed at 140 ℃ for 5 hours. The solution was cooled in an ice bath for 1. 5 hours. The crystals formed are filtered, washed with a small amount of ice-cold water and dried in vacuum. Distill about 80 cm3 filtrate, cool the solution in ice to produce another batch of crystals, wash and dry as mentioned above to obtain 3-bromo-2-bromomethylpropionic acid. |