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68097-75-6

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68097-75-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68097-75-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,9 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 68097-75:
(7*6)+(6*8)+(5*0)+(4*9)+(3*7)+(2*7)+(1*5)=166
166 % 10 = 6
So 68097-75-6 is a valid CAS Registry Number.

68097-75-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-4-(piperidin-1-ylmethyl)phenol

1.2 Other means of identification

Product number -
Other names 2-Methyl-4-piperidinomethyl-phenol

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:68097-75-6 SDS

68097-75-6Relevant articles and documents

Synthesis and biological evaluation of a new class of multi-target heterocycle piperazine derivatives as potential antipsychotics

Gao, Lanchang,Hao, Chao,Ma, Ru,Chen, Jiali,Zhang, Guisen,Chen, Yin

, p. 16931 - 16941 (2021/05/25)

In this study, we designed and synthesized a novel series of multi-receptor ligands as polypharmacological antipsychotic agents by using a multi-receptor affinity strategy. Among them,3wcombines a multi-receptor mechanism with high mixed affinities for D

Alkyl- and alkoxy-substituted lamtidine analogues: Synthesis and H2-antagonistic activity. 38th Communication: H2-antihistaminics

Bonjean,Schunack

, p. 501 - 507 (2007/10/02)

In studies on the structure-activity relationships of histamine H2-receptor antagonists, lamtidine analogous derivatives of ortho-, meta- and para-substituted piperidinomethylphenoxypropylamines bearing an additional substituent on the aromatic

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