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Merck

22880

Sigma-Aldrich

Chloroacetyl chloride

purum, ≥99.0% (GC)

Sinónimos:

Chloroacetic chloride

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About This Item

Fórmula lineal:
ClCH2COCl
Número de CAS:
Peso molecular:
112.94
Beilstein/REAXYS Number:
605439
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

3.9 (vs air)

Quality Level

vapor pressure

60 mmHg ( 41.5 °C)

grade

purum

assay

≥99.0% (GC)

form

liquid

refractive index

n20/D 1.453 (lit.)
n20/D 1.453

bp

105-106 °C (lit.)

mp

−22 °C (lit.)

solubility

water: insoluble

density

1.419 g/mL at 20 °C
1.418 g/mL at 25 °C (lit.)

functional group

acyl chloride

SMILES string

ClCC(Cl)=O

InChI

1S/C2H2Cl2O/c3-1-2(4)5/h1H2

InChI key

VGCXGMAHQTYDJK-UHFFFAOYSA-N

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General description

Chloroacetyl chloride is an aliphatic acid chloride.

Application

Chloroacetyl chloride may be used to prepare:
  • 2-chloro-N-(pyridine-2-yl)acetamide via N-acylation of pyridin-2-amine
  • chloroacetyl cellulose by reacting with cellulose in N,N-dimethylformamide
  • azetobenzothiazine derivatives by reacting with 1,3-benzothiazines in the presence of a base in refluxing toluene
  • 2-chloro-1-(3,5-diaryl-4,5-dihydropyrazol-1-yl)-ethanones by reacting with 3,5-diaryl-4,5-dihydropyrazoles
  • chloroacetyl isatins by reacting with isatins under microwave conditions
It acts as a linker during the grafting of pyrimethanil with chitosan.
Chloroacetyl chloride was used in the synthesis of N-hydrazino acetyl-sulphonamides.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Eye Dam. 1 - Skin Corr. 1A - STOT RE 1

target_organs

Lungs

supp_hazards

Storage Class

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

wgk_germany

WGK 3

flash_point_f

212.0 °F - closed cup

flash_point_c

100 °C - closed cup

ppe

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


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Visite la Librería de documentos

Synthesis and Anticancer Activity of Isatin-Based Pyrazolines and Thiazolidines Conjugates.
Havrylyuk D, et al.
Arch. Pharm. (Weinheim), 344(8), 514-522 (2011)
Application of microwave induced Delepine reaction to the facile one pot synthesis of 7-substituted 1, 3-dihydro-2h-[1, 4]-benzodiazepin-2-one-5-methyl carboxylates from the corresponding 1-chloroacetyl isatins.
Sharma P, et al.
International Journal of Chemical Sciences, 8(1) (2010)
Oana Maria Parasca et al.
Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi, 117(1), 238-243 (2014-02-11)
Infections caused by bacterial species are common in immunocompromised patients and carry significant treatment costs and mortality. The emerging resistance of microorganisms to some synthetic antimicrobial agents makes it necessary to continue the research for new antimicrobial drugs. To design
Novel indole syntheses by ring transformation of ?-lactam-condensed 1, 3-benzothiazines into indolo [2, 3-b][1, 4] benzothiazepines and indolo [3, 2-c] isoquinolines.
Fodor L, et al.
Tetrahedron, 68(3), 851-856 (2012)
Amination and thiolation of chloroacetyl cellulose through reactive dissolution in N, N-dimethylformamide.
Labafzadeh SR, et al.
Carbohydrate Polymers, 116, 60-66 (2015)

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