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Benzenemethanol, α-methyl-2-(1H-tetrazol-5-yl)-, also known as α-methyl-2-(1H-tetrazol-5-yl)benzenemethanol, is an organic compound with the chemical formula C9H11N3O. It is a derivative of benzyl alcohol, featuring a methyl group attached to the α-carbon and a 1H-tetrazol-5-yl group at the 2-position. Benzenemethanol, a-methyl-2-(1H-tetrazol-5-yl)- is characterized by its tetrazol-5-yl ring, which is a five-membered heterocyclic ring containing four nitrogen atoms and one hydrogen atom. Benzenemethanol, α-methyl-2-(1H-tetrazol-5-yl)-, is a white crystalline solid and is used in various chemical reactions and as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Its unique structure and properties make it a valuable building block in the development of new drugs and materials.

138944-16-8

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138944-16-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138944-16-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,4 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 138944-16:
(8*1)+(7*3)+(6*8)+(5*9)+(4*4)+(3*4)+(2*1)+(1*6)=158
158 % 10 = 8
So 138944-16-8 is a valid CAS Registry Number.

138944-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-(1H-Tetrazol-5-yl)-phenyl]-ethanol

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

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More Details:138944-16-8 SDS

138944-16-8Downstream Products

138944-16-8Relevant academic research and scientific papers

Directed metalation and new synthetic transformations of 5-aryltetrazoles

Flippin, Lee A.

, p. 6857 - 6860 (1991)

The tetrazole moiety is a useful directing group for the lithiation of 5-aryl substituents. Dilithiated 5-aryltetrazoles generally react with alkyl halides and aldehydes to give substitution and addition products, respectively.

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