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硫代苯甲酰胺

硫代苯甲酰胺用途

化工、药物中间体。

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硫代苯甲酰胺名称

[ CAS 号 ]:
2227-79-4

[ 中文名 ]:
硫代苯甲酰胺

[ 英文名 ]:
Thiobenzamide

[英文别名 ]:

硫代苯甲酰胺物理化学性质

[ 密度 ]:
1.2±0.1 g/cm3

[ 沸点 ]:
245.0±23.0 °C at 760 mmHg

[ 熔点 ]:
113-117 °C(lit.)

[ 分子式 ]:
C7H7NS

[ 分子量 ]:
137.202

[ 闪点 ]:
102.0±22.6 °C

[ 精确质量 ]:
137.029922

[ PSA ]:
58.11000

[ LogP ]:
1.49

[ 外观性状 ]:
淡黄色-绿色结晶粉末

[ 蒸汽压 ]:
0.0±0.5 mmHg at 25°C

[ 折射率 ]:
1.653

[ 储存条件 ]:
通风低温干燥,与库房食品原料分开存放

硫代苯甲酰胺MSDS

硫代苯甲酰胺毒性和生态

CHEMICAL IDENTIFICATION

RTECS NUMBER :
CV5860000
CHEMICAL NAME :
Benzamide, thio-
CAS REGISTRY NUMBER :
2227-79-4
LAST UPDATED :
199806
DATA ITEMS CITED :
7
MOLECULAR FORMULA :
C7-H7-N-S
MOLECULAR WEIGHT :
137.21
WISWESSER LINE NOTATION :
ZYR&US

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
95 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
500 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
6300 mg/kg/15W-C
TOXIC EFFECTS :
Tumorigenic - equivocal tumorigenic agent by RTECS criteria Liver - multiple effects Liver - tumors
TYPE OF TEST :
TD - Toxic dose (other than lowest)
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
13 gm/kg/38W-C
TOXIC EFFECTS :
Tumorigenic - equivocal tumorigenic agent by RTECS criteria Liver - tumors
TYPE OF TEST :
TD - Toxic dose (other than lowest)
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
13300 mg/kg/38W-C
TOXIC EFFECTS :
Tumorigenic - equivocal tumorigenic agent by RTECS criteria Liver - tumors

MUTATION DATA

TEST SYSTEM :
Rodent - mouse
DOSE/DURATION :
180 umol/kg
REFERENCE :
MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 192,141,1987
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硫代苯甲酰胺安全信息

[ 符号 ]:

GHS06

[ 信号词 ]:
Danger

[ 危害声明 ]:
H301

[ 警示性声明 ]:
P301 + P310

[ 个人防护装备 ]:
Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges

[ 危害码 (欧洲) ]:
Xn:Harmful;

[ 风险声明 (欧洲) ]:
R25

[ 安全声明 (欧洲) ]:
S45

[ 危险品运输编码 ]:
UN 2811 6.1/PG 3

[ WGK德国 ]:
3

[ RTECS号 ]:
CV5860000

[ 包装等级 ]:
III

[ 危险类别 ]:
6.1

[ 海关编码 ]:
2930909090

硫代苯甲酰胺合成路线

硫代苯甲酰胺海关

[ 海关编码 ]: 2930909090

[ 中文概述 ]:
2930909090. 其他有机硫化合物. 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

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

硫代苯甲酰胺文献

Cytotoxic activity of 3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl)chromen-4-ones and 4-oxo-4H-chromene-3-carbothioic acid N-phenylamides.

Eur. J. Med. Chem. 45 , 790-4, (2010)

6/6,7-Substituted-3-formylchromones (8a-g) were reacted with 2 equivalents thiobenzamide (9) in refluxing toluene to furnish substituted-3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl)chromen-4-ones (10a-g) in ...

Potent inhibition of alcohol self-administration in alcohol-preferring rats by a κ-opioid receptor antagonist.

J. Pharmacol. Exp. Ther. 350(1) , 171-80, (2014)

A substituted aryl amide derivative of 6-naltrexamine--17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-[(4'-trimethylfluoro)benzamido]morphinan-hydrochloride--(compound 5), previously shown to be a...

Facile synthesis of nitriles via manganese oxide promoted oxidative dehydrosulfurization of primary thioamides.

Chem. Commun. (Camb.) 48(91) , 11247-9, (2012)

In the presence of manganese oxides, dehydrosulfurization of various kinds of primary thioamides including aromatic, heterocyclic, and aliphatic ones efficiently proceeded to give the corresponding ni...


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