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Merck
CN

169897

Sigma-Aldrich

1-苯基-1H-四唑-5-硫醇

98%

别名:

1-苯基-5-巯基四氮唑, 1-苯基四氮唑-5-硫醇, 5-巯基-1-苯基四氮唑

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About This Item

经验公式(希尔记法):
C7H6N4S
CAS号:
分子量:
178.21
Beilstein:
139068
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

方案

98%

表单

powder

mp

145 °C (dec.) (lit.)

溶解性

ethanol: soluble 5%, clear, colorless to faintly yellow

SMILES字符串

Sc1nnnn1-c2ccccc2

InChI

1S/C7H6N4S/c12-7-8-9-10-11(7)6-4-2-1-3-5-6/h1-5H,(H,8,10,12)

InChI key

GGZHVNZHFYCSEV-UHFFFAOYSA-N

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一般描述

1-Phenyl-1H-tetrazole-5-thiol is an effective inhibitor of aluminum corrosion in 1M HCl solution.

应用

1-Phenyl-1H-tetrazole-5-thiol was used in the synthesis of oxacyclic building blocks via highly stereoselective radical cyclization and olefin metathesis reactions. It was also used in the synthesis of metalated tetradecyl sulfone.

象形图

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警示用语:

Danger

危险分类

Aquatic Chronic 4 - Eye Irrit. 2 - Flam. Sol. 1 - Skin Sens. 1

储存分类代码

4.1A - Other explosive hazardous materials

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

监管及禁止进口产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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The inhibitive effect of some tetrazole derivatives towards Al corrosion in acid solution: Chemical, electrochemical and theoretical studies.
Khaled KF and Al-Qahtani MM.
Materials Chemistry and Physics, 113(1), 150-158 (2009)
A formal synthesis of 3-O-(4-methoxybenzyl)-azidosphingosine by a modified Julia olefination.
Compostella F, et al.
Tetrahedron, 58(22), 4425-4428 (2002)
Total synthesis of ambruticin.
Eun Lee et al.
Angewandte Chemie (International ed. in English), 41(1), 176-178 (2002-12-20)
K Nesmĕrák et al.
Folia microbiologica, 45(2), 138-142 (2001-03-29)
The antifungal effect of substituted 1-phenyl-5-mercaptotetrazoles was tested with Candida tropicalis, C. pseudotropicalis, C. mogii, Trichosporon cutaneum, Cryptococcus albidus and S. cerevisiae. Candida strains exhibited the lowest sensitivity to the compounds; the most sensitive was S. cerevisiae. The MIC values
J Kejha et al.
Ceskoslovenska farmacie, 39(7), 294-298 (1990-09-01)
For the investigation of new anti-inflammatory drugs, 1-phenyl-5-mercaptotetrazole (I) was selected as the principal structure. The purpose itself lay in an alkylation of the mercapto group with different remainders. In some cases at the same time a substituent was introduced

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