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2H-Tetrazole, 5-(chloromethyl)-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55408-14-5

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55408-14-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55408-14-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,0 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55408-14:
(7*5)+(6*5)+(5*4)+(4*0)+(3*8)+(2*1)+(1*4)=115
115 % 10 = 5
So 55408-14-5 is a valid CAS Registry Number.

55408-14-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(chloromethyl)-2-methyltetrazole

1.2 Other means of identification

Product number -
Other names 5-chloromethyl-2-methyl-2H-tetrazole

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:55408-14-5 SDS

55408-14-5Relevant academic research and scientific papers

High affinity phenylglycinol-based NK1 receptor antagonists

Owens,Harrison,Moseley,Swain,Sadowski,Cascieri

, p. 51 - 56 (1998)

Heterocyclic replacements for the carboxamido group of the previously disclosed phenylglycinol-based human NK1 (hNK1) receptor antagonists have been investigated, ultimately leading to acyclic compounds with sub-nanomolar affinity for the hNK1 receptor.

NOVEL GLUCOKINASE ACTIVATORS AND METHODS OF USING SAME

-

Page/Page column 78, (2008/06/13)

Compounds are provided which are phosphonate and phosphinate activators and thus are useful in treating diabetes and related diseases and have the structure wherein is a heteroaryl ring; R4 is —(CH2)n-Z-(CH2)m—PO(OR7)(OR8), —(CH2)nZ-(CH2)m—PO(OR7)Rg, —(CH2)n-Z-(CH2)m—OPO(OR7)Rg, —(CH2)nZ—(CH2)m—OPO(R9)(R10), or —(CH2)nZ—(CH2)m—PO(R9)(R10);R5 and R6 are independently selected from H, alkyl and halogen;Y is R7(CH2)s or is absent; andX, n, Z, m, R4, R5, R6, R7, and s are as defined herein; or a pharmaceutically acceptable salt thereof. A method for treating diabetes and related diseases employing the above compounds is also provided.

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