D152803
二甲氨基甲酰氯
98%
别名:
二甲基氨基甲酰氯, 氯代甲酰基二甲胺
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关于此项目
线性分子式:
(CH3)2NCOCl
化学文摘社编号:
分子量:
107.54
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-208-6
Beilstein/REAXYS Number:
878197
MDL number:
Assay:
98%
Form:
liquid
产品名称
二甲氨基甲酰氯, 98%
InChI
1S/C3H6ClNO/c1-5(2)3(4)6/h1-2H3
InChI key
YIIMEMSDCNDGTB-UHFFFAOYSA-N
SMILES string
CN(C)C(Cl)=O
assay
98%
form
liquid
refractive index
n20/D 1.453 (lit.)
bp
167-168 °C/775 mmHg (lit.)
mp
−33 °C (lit.)
density
1.168 g/mL at 25 °C (lit.)
Quality Level
Application
二甲基氨基甲酰氯可用于合成：
- 苄基苯酚中的双取代氨基甲酸酯。
- 通过与异烟酸 N -氧化物和氰化锌反应生成2-氰基异烟酰胺。采用该方法合成一种新型黄嘌呤氧化还原酶抑制剂。
- 乙酰胆碱酯酶 (AChE) 和 5-羟色胺转运体 (SERT) 双重抑制剂。
signalword
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 1B - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
179.6 °F - closed cup
flash_point_c
82 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Design and synthesis of dual inhibitors of acetylcholinesterase and serotonin transporter targeting potential agents for Alzheimer's disease.
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Zinc cyanide mediated direct α-cyanation of isonicotinic acid N-oxide. Application to the synthesis of FYX-051, a xanthine oxidoreductase inhibitor.
Huo Z, et al.
Tetrahedron Letters, ?49(28), 4369-4371 (2008)
A R Sellakumar et al.
Journal of environmental pathology and toxicology, 4(1), 107-115 (1980-08-01)
The comparative carcinogenicity of dimethylcarbamoyl chloride (DMCC) was studies in male, Syrian Golden Hamsters by inhalation. Hamsters were exposed to 1ppm and the exposure periods were 6 hours per day, 5 days per week for the lifetime of the animals.
C A Snyder et al.
Cancer letters, 33(2), 175-181 (1986-11-01)
Three direct-acting carcinogens, beta-propiolactone (BPL), methylmethane sulfonate (MMS), and dimethylcarbamyl chloride (DMCC), were evaluated for their carcinogenic potencies in the nasal mucosa of rats and for their abilities to bind in vivo to rat nasal mucosal DNA. The relative carcinogenic
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