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14832-58-7

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14832-58-7 Usage

Chemical Class

Tetrazole derivatives

Usage

Medicinal chemistry for potential pharmacological activities
+ Antihypertensive properties
+ Anticancer properties
+ Antimicrobial properties

Specific Target

Inhibits the angiotensin-converting enzyme (ACE)
+ Role in regulating blood pressure

Promise

Inhibiting cancer cell growth and fighting microbial pathogens

Unique Features

Diverse biological activities and interesting target for further research
+ Potential development as a pharmaceutical agent

Check Digit Verification of cas no

The CAS Registry Mumber 14832-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,3 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14832-58:
(7*1)+(6*4)+(5*8)+(4*3)+(3*2)+(2*5)+(1*8)=107
107 % 10 = 7
So 14832-58-7 is a valid CAS Registry Number.

14832-58-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-2H-tetrazol-5-amine

1.2 Other means of identification

Product number -
Other names N-benzyl-1H-tetrazol-5-amine

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:14832-58-7 SDS

14832-58-7Relevant articles and documents

Anodic Oxidation of Aminotetrazoles: A Mild and Safe Route to Isocyanides

Leech, Matthew C.,Petti, Alessia,Tanbouza, Nour,Mastrodonato, Andrea,Goodall, Iain C. A.,Ollevier, Thierry,Dobbs, Adrian P.,Lam, Kevin

, p. 9371 - 9375 (2021/12/09)

A new electrochemical method for the preparation of isocyanides from easily accessible aminotetrazole derivatives has been developed, which tolerates an unprecedented range of functional groups. The use of chemical, rather than electrochemical, oxidation to afford isocyanides was also demonstrated, which provides access to these compounds for those without electrosynthesis equipment. The practicality of scale-up using flow electrochemistry has been demonstrated, in addition to the possibility of using electrochemically generated isocyanides in further reactions.

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