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431656

Sigma-Aldrich

Tribromoacetyl chloride

97%

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About This Item

Linear Formula:
CBr3COCl
CAS Number:
34718-47-3
Molecular Weight:
315.19
MDL number:
MFCD00209618
UNSPSC Code:
12352100
PubChem Substance ID:
24867039
NACRES:
NA.22

vapor pressure

0.23 psi ( 20 °C)

Assay

97%

form

liquid

refractive index

n20/D 1.583 (lit.)

density

1.628 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

ClC(=O)C(Br)(Br)Br

InChI

1S/C2Br3ClO/c3-2(4,5)1(6)7

InChI key

RDBMNMVDVKRYKW-UHFFFAOYSA-N

Application

Tribromoacetyl chloride may be used for the preparation of dihexadecyl N-(tribromoacetyl)-L-glutamate.[1] It may be used for the synthesis of docetaxel.[2]

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBD2716V
15411HU
14711LA
09904MG
14012PS

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A novel two-dimensional photopolymerization at an oriented bilayer surface. Effective molecular-weight control using membrane state and chain transfer.
Higashi, N, et al.
Macromolecules, 23(5), 1475-1480 (1990)
Development of New Efficient Synthetic Methods for Docetaxel.
Heo JH, et al.
ChemInform, 40(29) (2009)
Cycloaddition of dihaloketenes with trimethylsiloxycycloolefins and fluorination of the products.
Habibi MH, et al.
Journal of Fluorine Chemistry, 37(2), 177-181 (1987)
Study of the Cine-Rearrangement and the Cinesubstitution of 2, 2-Dihalocyclobutanones.
Jose'Renato Cagnon JMB.
Journal of the Brazilian Chemical Society, 7(5), 371-377 (1996)
Laser Raman and infrared spectra of tribromoacetyl-chloride.
Randhawa HS and Walter W.
Journal of Molecular Structure, 35(2), 303-307 (1976)

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