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Merck

D152803

Sigma-Aldrich

Dimethylcarbamoylchlorid

98%

Synonym(e):

Chlorameisensäure-dimethylamid

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About This Item

Lineare Formel:
(CH3)2NCOCl
CAS-Nummer:
Molekulargewicht:
107.54
Beilstein:
878197
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Qualitätsniveau

Assay

98%

Form

liquid

Brechungsindex

n20/D 1.453 (lit.)

bp

167-168 °C/775 mmHg (lit.)

mp (Schmelzpunkt)

−33 °C (lit.)

Dichte

1.168 g/mL at 25 °C (lit.)

SMILES String

CN(C)C(Cl)=O

InChI

1S/C3H6ClNO/c1-5(2)3(4)6/h1-2H3

InChIKey

YIIMEMSDCNDGTB-UHFFFAOYSA-N

Anwendung

Dimethylcarbamyl chloride can be used to synthesize:
  • Disubstituted carbamates from benzylphenols.
  • 2-Cyanoisonicotinamide by reacting with isonicotinic acid N-oxide and zinc cyanide. This method was adopted to synthesize a novel xanthine oxidoreductase inhibitor.
  • Acetylcholinesterase (AChE) and serotonin transporter (SERT) dual inhibitors.

Piktogramme

Skull and crossbonesHealth hazard

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 1B - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

179.6 °F - closed cup

Flammpunkt (°C)

82 °C - closed cup

Persönliche Schutzausrüstung

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


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Design and synthesis of dual inhibitors of acetylcholinesterase and serotonin transporter targeting potential agents for Alzheimer's disease.
Kogen H, et al.
Organic Letters, 4(20), 3359-3362 (2002)
Dimethylcarbamoyl chloride.
Report on carcinogens : carcinogen profiles, 10, 106-107 (2004-08-25)
S J Garte et al.
Environmental health perspectives, 81, 29-31 (1989-05-01)
Techniques of molecular biology have been used to determine the relationship of cellular oncogenes to mechanisms of experimental carcinogenesis. Model systems involving three direct-acting alkylating carcinogens, two organ sites, and two species have been employed to elucidate the relationships between
A E Hochwalt et al.
Molecular carcinogenesis, 1(1), 4-6 (1988-01-01)
Rat nasal squamous cell carcinomas induced by inhalation of three direct-acting alkylating agents yielded DNA containing activated oncogenes with no homology to any member of the ras family. The novel NIH 3T3 transforming oncogenes from tumors induced by beta-propiolactone and
C A Snyder et al.
Archives of toxicology, 61(1), 3-6 (1987-01-01)
A new inhalation exposure system has been developed which allows the determination of inhaled doses of vapors and gases by laboratory rats. The system consists of saran bags connected to head-only exposure cylinders via one-way valves. One bag serves as

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