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CasNo: 598-72-1
Molecular Formula: C3H5BrO2
Appearance: clear colorless to yellowish liquid after melting
|
Preparation |
2-Bromopropionic acid is obtained by bromination of propionic acid. Add propionic acid and phosphorus trichloride to the reaction kettle, keep the temperature at 80°C, slowly add bromine to the reaction solution dropwise, and heat up to 85°C after the addition of bromine, and raise the temperature to 100°C when the color of bromine disappears completely, it takes about 2~3h, and then the bromine and hydrobromic acid are recovered under reduced pressure, and then the finished product is obtained by distillation under reduced pressure. |
|
Application |
2-bromopropionic acid is an organic synthesis intermediate, used in the production of herbicides quizalofop-ethyl, napropamide, fenthiaprop and fungicides metalaxyl, benalaxyl, procymidone, etc., used in the synthesis of pharmaceutical intermediates body alanine. |
InChI:InChI=1/C3H5BrO2/c1-2(4)3(5)6/h2H,1H3,(H,5,6)/p-1/t2-/m0/s1
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C9H7BrN2O6
2,4-Dinitrophenol
2-Bromopropionic acid
| Conditions | Yield |
|---|---|
|
With
water;
|
propionic acid
3-Bromopropionic acid
chloropropionic acid
2-Bromopropionic acid
(R,S)-2-chloropropionic acid
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride; oxygen; potassium bromide; sodium nitrite;
In
chloroform; water;
at 40 ℃;
for 18h;
under 760.051 Torr;
Sealed tube;
Irradiation;
|
65% 23% |
LACTIC ACID
1,1-dibromopropene
carbon tetrabromide
propionic acid
Methyl 2-bromopropionate
2-(2-benzimidazolylthio)propionic acid
2-(1-methyl-1H-benzimidazol-2-ylmercapto)-propionic acid
2-(5-chloro-1(3)H-benzimidazol-2-ylmercapto)-propionic acid