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About This Item
Linear Formula:
BrCH2CHBrCOCl
CAS Number:
Molecular Weight:
250.32
Beilstein:
1749801
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
Assay
97%
form
liquid
refractive index
n20/D 1.542 (lit.)
bp
191-193 °C (lit.)
density
2.181 g/mL at 25 °C (lit.)
SMILES string
ClC(=O)C(Br)CBr
InChI
1S/C3H3Br2ClO/c4-1-2(5)3(6)7/h2H,1H2
InChI key
HWKWYDXHMQQDQJ-UHFFFAOYSA-N
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Application
2,3-Dibromopropionyl chloride was used in synthesis of:
- series of 2,3-diaminopropionanilides
- enantiomers of 1,4-dideoxy-1,4-iminolyxitol and 1,4-dideoxy-1,4-iminoribitol
- acromelic acid A
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
150.8 °F - closed cup
Flash Point(C)
66 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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P A Tenthorey et al.
Journal of medicinal chemistry, 24(9), 1059-1063 (1981-09-01)
A series of 2,3-diaminopropionanilides was synthesized by acylation of mono- and disubstituted aniline derivatives with 2,3-dibromopropionyl chloride and subsequent amination with the appropriate secondary amines. The target compounds were evaluated in mice for antiarrhythmic efficacy against chloroform-induced tachycardia and for
Concise enantioselective synthesis of acromelic acid A.
Takano S, et al.
Journal of the American Chemical Society, 109(18), 5523-5524 (1987)
Chiral synthesis of both enantiomers of 1, 4-dideoxy-1, 4-immolyxitol and 1, 4-dideoxy-1, 4-iminoribitol.
Takano S, et al.
Tetrahedron Asymmetry, 3(6), 681-684 (1992)
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