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22347-34-8

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22347-34-8 Usage

General Description

1-(4-Sulfamoylphenyl)-5-mercaptotetrazole is a chemical compound with the molecular formula C9H8N6O2S2. It is a sulfonamide derivative and contains both a sulfonamide group and a mercaptotetrazole group. 1-(4-Sulfamoylphenyl)-5-mercaptotetrazole is a potential antimicrobial agent and has been studied for its antibacterial and antifungal properties. It has also been investigated for its potential use in the treatment of various diseases, including cancer and inflammatory conditions. Additionally, 1-(4-Sulfamoylphenyl)-5-mercaptotetrazole has been studied for its potential use as a corrosion inhibitor in the oil and gas industry. Overall, this compound has shown promise in various applications, and further research is ongoing to explore its potential uses and benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 22347-34-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,4 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22347-34:
(7*2)+(6*2)+(5*3)+(4*4)+(3*7)+(2*3)+(1*4)=88
88 % 10 = 8
So 22347-34-8 is a valid CAS Registry Number.

22347-34-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(5-sulfanylidene-2H-tetrazol-1-yl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:22347-34-8 SDS

22347-34-8Downstream Products

22347-34-8Relevant articles and documents

Kinetics and Mechanism of the Alkaline Release of Phenyl(mercapto)tetrazoles from α-Oximes

Boggs, Roger A.,Hasan, Fariza B.,Mahoney, J. Barry,Mehta, Avi C.,Palumbo, Catherine M. K.,et al.

, p. 1271 - 1277 (2007/10/02)

Compounds such as α-phenyl(mercapto)tetrazole (PMT) oxime (9) undergo rapid elimination of the PMT anion in base via a nitrosoene intermediate.Solution kinetics and HPLC analysis of reaction products are consistent with the mechanism shown in Scheme 2.For open chain oximes such as 4, substitution α to the oxime increases the rate of release of PMT and is attributed to the relief of strain when a crowded reactant is converted to a less-crowded product.For cyclic oximes, the six-membered ring compounds are more reactive than the corresponding five-membered compounds.A linear isokinetic relationship between the entropy and enthalpy of activation was found with β = 346 +/- 51 K.Entropies of activation were found to range from -7 to +24 c.u. (1 c.u. = 4.184 J mol-1 K-1) and support the proposed mechanism.

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