2,2,2-三氯乙酰胺
2,2,2-三氯乙酰胺用途
用作有机合成原料、医药中间体
2,2,2-三氯乙酰胺名称
[ CAS 号 ]:
594-65-0
[ 中文名 ]:
2,2,2-三氯乙酰胺
[ 英文名 ]:
2,2,2-Trichloroacetamide
[中文别名 ]:
[英文别名 ]:
- Acetamide, 2,2,2-trichloro-
- TRICHLOROACETAMIDE
- 2,2,2-Trichloroacetamide
- 3,3,3-trichloroacetamide
- chloraloxime
- 2,2,2-Chloroacetamide
- a,a,a-Trichloroacetamide
- trichloro-acetic acid amide
- 2,2,2-Trichloroaceta
- trichloroacetyl amide
2,2,2-三氯乙酰胺物理化学性质
[ 密度 ]:
1.7±0.1 g/cm3
[ 沸点 ]:
239.0±0.0 °C at 760 mmHg
[ 熔点 ]:
139-141 °C(lit.)
[ 分子式 ]:
C2H2Cl3NO
[ 分子量 ]:
162.402
[ 闪点 ]:
88.5±25.9 °C
[ 精确质量 ]:
160.920197
[ PSA ]:
43.09000
[ LogP ]:
1.15
[ 外观性状 ]:
白色固体
[ 蒸汽压 ]:
0.0±0.4 mmHg at 25°C
[ 折射率 ]:
1.521
[ 储存条件 ]:
室温
[ 稳定性 ]:
Stable. Incompatible with strong acids, strong bases, strong oxidizing agents, strong reducing agents.
[ 水溶解性 ]:
13 g/L (20 ºC)
2,2,2-三氯乙酰胺MSDS
2,2,2-三氯乙酰胺毒性和生态
CHEMICAL IDENTIFICATION
- RTECS NUMBER :
- AC9275000
- CHEMICAL NAME :
- Acetamide, 2,2,2-trichloro-
- CAS REGISTRY NUMBER :
- 594-65-0
- BEILSTEIN REFERENCE NO. :
- 1754028
- LAST UPDATED :
- 199701
- DATA ITEMS CITED :
- 5
- MOLECULAR FORMULA :
- C2-H2-Cl3-N-O
- MOLECULAR WEIGHT :
- 162.40
- WISWESSER LINE NOTATION :
- ZVXGGG
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
- TYPE OF TEST :
- LDLo - Lowest published lethal dose
- ROUTE OF EXPOSURE :
- Oral
- SPECIES OBSERVED :
- Rodent - rat
- DOSE/DURATION :
- 500 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- REFERENCE :
- JPETAB Journal of Pharmacology and Experimental Therapeutics. (Williams & Wilkins Co., 428 E. Preston St., Baltimore, MD 21202) V.1- 1909/10- Volume(issue)/page/year: 90,260,1947
- TYPE OF TEST :
- LDLo - Lowest published lethal dose
- ROUTE OF EXPOSURE :
- Intraperitoneal
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 1100 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- REFERENCE :
- JACSAT Journal of the American Chemical Society. (American Chemical Soc., Distribution Office Dept. 223, POB 57136, West End Stn., Washington, DC 20037) V.1- 1879- Volume(issue)/page/year: 63,1437,1941
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intravenous
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 180 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- REFERENCE :
- CSLNX* U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. (Aberdeen Proving Ground, MD 21010) Volume(issue)/page/year: NX#04129 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X1039 No. of Facilities: 16 (estimated) No. of Industries: 2 No. of Occupations: 2 No. of Employees: 262 (estimated) No. of Female Employees: 82 (estimated)
2,2,2-三氯乙酰胺安全信息
[ 符号 ]:
GHS07
[ 信号词 ]:
Warning
[ 危害声明 ]:
H319
[ 警示性声明 ]:
P305 + P351 + P338
[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves
[ 危害码 (欧洲) ]:
Xn:Harmful;
[ 风险声明 (欧洲) ]:
R22;R36/37/38
[ 安全声明 (欧洲) ]:
S36/37-S45-S37/39-S26
[ 危险品运输编码 ]:
UN 2811 6.1/PG 3
[ WGK德国 ]:
3
[ RTECS号 ]:
AC9275000
[ 危险类别 ]:
6.1
[ 海关编码 ]:
29241900
2,2,2-三氯乙酰胺合成路线
2,2,2-三氯乙酰胺上下游产品
2,2,2-三氯乙酰胺上游产品
2,2,2-三氯乙酰胺下游产品
2,2,2-三氯乙酰胺海关
[ 海关编码 ]: 2924199090
[ 中文概述 ]:
2924199090. 其他无环酰胺(包括无环氨基甲酸酯)(包括其衍生物及盐). 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:30.0%
[ 申报要素 ]: 品名, 成分含量, 用途, 包装
[ Summary ]:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
2,2,2-三氯乙酰胺文献
J. Org. Chem. 78(4) , 1699-705, (2013)
We describe an improved synthesis of (-)-5,11-dideoxytetrodotoxin from an enone, which was used for synthesis of tetrodotoxin and its analogues in this laboratory. One of the major modifications was t...
Activation of glycosyl trichloroacetimidates with perchloric acid on silica (HClO(4)-SiO(2)) provides enhanced alpha-selectivity.Carbohydr. Res. 345(14) , 2074-8, (2010)
Obtaining high stereoselectivity in glycosylation reactions is often challenging in the absence of neighboring group participation. In this study, we demonstrate that activation of glycosyl trichloroa...
Synthetic studies toward the anthrax tetrasaccharide: alternative synthesis of this antigenCarbohydr. Res. 356 , 115-31, (2012)
The synthesis of the anthrax tetrasaccharide, amenable for conjugation, has been envisaged by both [2+2] and [1+3] approaches from D-fucose and L-rhamnose. The successful route reported herein relies ...
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