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N,N-dimethyl-2H-tetrazol-5-amine is an organic compound with the chemical formula C3H8N4. It is a derivative of the tetrazol-5-amine family, characterized by the presence of two methyl groups attached to the nitrogen atoms. This colorless solid is soluble in water and is commonly used as a reagent in the synthesis of tetrazolium salts, which are employed in various biological assays to measure cell viability and proliferation. Due to its reactivity, it is important to handle N,N-dimethyl-2H-tetrazol-5-amine with care, as it can be sensitive to moisture and heat.

5422-45-7

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5422-45-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5422-45-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5422-45:
(6*5)+(5*4)+(4*2)+(3*2)+(2*4)+(1*5)=77
77 % 10 = 7
So 5422-45-7 is a valid CAS Registry Number.

5422-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-2H-tetrazol-5-amine

1.2 Other means of identification

Product number -
Other names 5-Dimethyl-amino-tetrazol

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:5422-45-7 SDS

5422-45-7Relevant academic research and scientific papers

Fimctlonalized tetrazoles from cyanogen azide with secondary amines

Joo, Young-Hyuk,Shreeve, Jean'ne M.

experimental part, p. 3573 - 3578 (2009/10/26)

Secondary amines react with cyanogen azide at ambient temperature in water/acetonitrile to provide tetrazole derivatives directly. The scope and limitations with regard to steric hindrance of the amine are discussed. Although reaction yields are moderate, 29-81%, the cyanogen azide reactions provide a direct and versatile route to functionalized tetrazoles that: may be especially useful considering the diversity of amines suitable for this transformation.

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