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423920

Sigma-Aldrich

1-Phenyl-1H-tetrazole-5-thiol sodium salt

98%

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About This Item

Fórmula empírica (notación de Hill):
C7H5N4NaS
Número de CAS:
15052-19-4
Peso molecular:
200.20
EC Number:
239-121-0
MDL number:
MFCD00051320
UNSPSC Code:
12352100
PubChem Substance ID:
24866539
NACRES:
NA.22

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.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
10730CN
06414DG
13523AN
09328DU

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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
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
[Information from the Soviet Toxicology Center].
Gigiena truda i professional'nye zabolevaniia, (10)(10), 55-56 (1980-10-01)

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