423920
1-苯基-1H-四唑-5-硫醇 钠盐
98%
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关于此项目
经验公式（希尔记法）:
C7H5N4NaS
化学文摘社编号:
分子量:
200.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
239-121-0
MDL number:
Assay:
98%
assay
98%
mp
>300 °C (lit.)
solubility
water: soluble 1g/15ml, clear
SMILES string
[Na]Sc1nnnn1-c2ccccc2
InChI
1S/C7H6N4S.Na/c12-7-8-9-10-11(7)6-4-2-1-3-5-6;/h1-5H,(H,8,10,12);/q;+1/p-1
InChI key
RSZMKAPXKXEWBY-UHFFFAOYSA-M
General description
1-Phenyl-1H-tetrazole-5-thiol sodium salt is a tetrazole derivative. The kinetics of its reaction with Diel′s-Alder adducts of 1,4-benzoquinone has been investigated.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Kinetics of the reaction of 1-phenyl-1H-tetrazole-5-thiol sodium salt with less substituted 1, 4-naphthoquinone 2, 3-epoxides.
O'Brien DF.
The Journal of Organic Chemistry, 33(1), 262-265 (1968)
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 423920-5G | 04061833323144 |