推荐产品
方案
≥97.0% (HPLC)
≥97.0%
表单
powder
质量
for spectrophotometric det. of Pd
for the determination of Bi
技术
UV/Vis spectroscopy: suitable
mp
145 °C (dec.) (lit.)
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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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
Fresenius Journal of Analytical Chemistry, 261, 151-151 (1972)
Mohammad M Khodaei et al.
The Journal of organic chemistry, 73(7), 2527-2532 (2008-03-05)
In the presence of 1-phenyl-5-mercaptotetrazole as a nucleophile, electrochemical oxidations of 1,2- and 1,4-dihydroxybenzenes have been investigated in aqueous solution using cyclic voltammetry and controlled-potential coulometry. The voltammetric results indicate that an electrooxidative/Michael-type sequential reaction occurs between the mercaptide anion
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
[Information from the Soviet Toxicology Center].
Gigiena truda i professional'nye zabolevaniia, (10)(10), 55-56 (1980-10-01)
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
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