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Merck
CN

151599

Trichloroacetyl chloride

99%

Synonym(s):

2,2,2-Trichloroacetyl chloride, Trichloroacetic acid chloride, Trichloroacetochloride

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About This Item

Linear Formula:
Cl3CCOCl
CAS Number:
76-02-8
Molecular Weight:
181.83
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24849149
EC Number:
200-926-7
Beilstein/REAXYS Number:
774120
MDL number:
MFCD00000792
Assay:
99%
Form:
liquid

Key Documents

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InChI key

PVFOMCVHYWHZJE-UHFFFAOYSA-N

InChI

1S/C2Cl4O/c3-1(7)2(4,5)6

SMILES string

ClC(=O)C(Cl)(Cl)Cl

vapor pressure

16 mmHg ( 20 °C)

assay

99%

form

liquid

Quality Level

200

bp

114-116 °C (lit.)

mp

−57 °C (lit.)

density

1.629 g/mL at 25 °C (lit.)

functional group

acyl chloride, chloro

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General description

Trichloroacetyl chloride, also known as 2,2,2-Trichloroacetyl chloride, is an asymmetric ketone that is commonly used as a source of chlorine atoms in laboratories and as an acylating agent to produce bis(trichloroacetyl) cyclic enamines.

Application

Trichloroacetyl chloride was used in the preparation of dihydro-1H-benzindoles. It was also used in the synthesis of 3-alkylbenzoxazolones.

signalword

Danger

flash_point_f

213.8 °F - open cup

flash_point_c

101 °C - open cup

ppe

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

pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A

Storage Class

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB5449
STBJ1769
STBG4836V
STBF8630V
STBD9326V

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Jianqiang Zhu et al.
The journal of physical chemistry. A, 121(36), 6800-6809 (2017-08-25)
Rate constants at room temperature (293 ± 2 K) and atmospheric pressure for the reaction of methyl n-propyl ether (MnPE), CH
A M Saillenfait et al.
Archives of toxicology, 70(2), 71-82 (1995-01-01)
The embryotoxicity of trichloroethylene (TRI), tetrachloroethylene (PER), and of four of their oxidative metabolites i.e. trichloroacetic acid, dichloroacetic acid, chloral hydrate, and trichloroacetyl chloride, was studied in vitro, using the rat whole embryo culture system. Embryos from Sprague-Dawley rats were
Ram N Ram et al.
The Journal of organic chemistry, 78(23), 11935-11947 (2013-10-31)
Benzoxazolone pharmacophore is present in clinical pharmaceuticals, drug candidates, and many compounds having a wide spectrum of biological activities. The methods available for the synthesis of benzoxazolones have limited diversity due to problems in accessibility and air-sensitivity of diversely substituted
Gustavo P Silveira et al.
The Journal of organic chemistry, 78(7), 3379-3383 (2013-03-14)
The first examples of dihydro-1H-benzindoles by enantioselective γ-lactamization reaction of naphthyl sulfilimines with trichloroacetyl chloride in the presence of ZnCu as catalyst (≥98:2 er and 65-80% yields) are described. Products are obtained by [3,3]-sigmatropic rearrangement of the azasulfonium enolate or
Hülya Senöz et al.
Chemical & pharmaceutical bulletin, 51(4), 444-447 (2003-04-04)
The pyrrolidine and morpholine enamines of cyclic ketones such as cyclohexanone and cyclopentanone were successfully diacetylated at alpha- and alpha'-positions with trichloroacetyl chloride using zinc catalyst. Morpholine enamines of the cyclic ketones gave acetylated morpholine in good yields besides the
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