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Merck

148229

Sigma-Aldrich

硫代苯甲酰胺

98%

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About This Item

线性分子式:
C6H5CSNH2
CAS号:
分子量:
137.20
Beilstein:
606021
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

98%

mp

113-117 °C (lit.)

官能基

amine
phenyl

SMILES 字串

NC(=S)c1ccccc1

InChI

1S/C7H7NS/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H2,8,9)

InChI 密鑰

QIOZLISABUUKJY-UHFFFAOYSA-N

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應用

硫代苯甲酰胺用于制备酰胺和脒加合物。它也用于合成 4-氧代-4H-亚甲基-3-碳硫代甲酸 N-苯酰胺

象形圖

Skull and crossbones

訊號詞

Danger

危險聲明

危險分類

Acute Tox. 3 Oral

儲存類別代碼

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

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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分析证书(COA)

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Yakov M Koen et al.
Chemical research in toxicology, 26(4), 564-574 (2013-03-08)
Thioacetamide (TA) has long been known as a hepatotoxicant whose bioactivation requires S-oxidation to thioacetamide S-oxide (TASO) and then to the very reactive S,S-dioxide (TASO2). The latter can tautomerize to form acylating species capable of covalently modifying cellular nucleophiles including
M M Simile et al.
Carcinogenesis, 17(7), 1533-1537 (1996-07-01)
S-Adenosyl-L-methionine (SAM) is a strong chemopreventive agent of rat liver carcinogenesis. Examination was made to determine whether inhibition by SAM of the development of preneoplastic liver lesions persists to SAM withdrawal in diethylnitrosamine-initiated F344 rats promoted with thiobenzamide (TB). The
W G Chung et al.
Molecules and cells, 7(6), 738-741 (1998-03-24)
Flavin-containing monooxygenase (FMO), known not to be induced by xenobiotics, has been induced by a polycyclic aromatic hydrocarbon, 3-methylcholanthrene (3MC). We have found a prominent augmentation of hepatic FMO1 both at transcription and translation levels by pretreatment of rats with
Presence of flavin-containing monooxygenase in rat brain.
S Bhamre et al.
Biochemical pharmacology, 42(2), 442-444 (1991-07-05)
T Mizutani et al.
Toxicology letters, 85(2), 101-105 (1996-05-01)
The hepatotoxicity of the 3 isomers of para-substituted thiobenzamides and the 3 isomers of 2-(para-substituted phenyl)-4-methylthiazoles was evaluated in mice depleted of glutathione (GSH) by pretreatment with buthionine sulfoximine (BSO). In accordance with previous studies with the rat, p-methoxythiobenzamide was

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