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Merck
CN

431656

Tribromoacetyl chloride

97%

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About This Item

Linear Formula:
CBr3COCl
CAS Number:
Molecular Weight:
315.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
liquid
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InChI

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

SMILES string

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

InChI key

RDBMNMVDVKRYKW-UHFFFAOYSA-N

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

Application

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

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

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

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

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Cycloaddition of dihaloketenes with trimethylsiloxycycloolefins and fluorination of the products.
Habibi MH, et al.
Journal of Fluorine Chemistry, 37(2), 177-181 (1987)
Development of New Efficient Synthetic Methods for Docetaxel.
Heo JH, et al.
ChemInform, 40(29) (2009)
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)
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)
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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