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1-Isoquinolinol, 1,2,3,4-tetrahydro-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114640-73-2

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114640-73-2 Usage

Structure

1-Isoquinolinol, 1,2,3,4-tetrahydro-2-methyl-

Type

Derivative of isoquinoline

Usage

Commonly used in the synthesis of various pharmaceuticals and organic compounds

Chelating agent

Known for its ability to act as a chelating agent

Medicinal applications

Studied for potential use as an antiviral and antitumor agent

Synthesis of heterocyclic compounds

Used in the synthesis of various heterocyclic compounds

Building block

A valuable building block in organic chemistry

Industrial applications

Found to have potential as a corrosion inhibitor

Check Digit Verification of cas no

The CAS Registry Mumber 114640-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,6,4 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 114640-73:
(8*1)+(7*1)+(6*4)+(5*6)+(4*4)+(3*0)+(2*7)+(1*3)=102
102 % 10 = 2
So 114640-73-2 is a valid CAS Registry Number.

114640-73-2SDS

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 2-methyl-3,4-dihydro-1H-isoquinolin-1-ol

1.2 Other means of identification

Product number -
Other names 1-hydroxy-2-methyl-1,2,3,4-tetrahydroisoquinoline

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:114640-73-2 SDS

114640-73-2Relevant academic research and scientific papers

Mercuric dehydrogenations of N-tertiary piperidine derivatives with different substitution pattern

Moehrle, H.,Claas, M.

, p. 749 - 753 (2007/10/02)

A comparison of the dehydrogenation of different N-tertiary piperidine derivatives with mercuric EDTA and mercuric acetate shows an increase of the reaction with the complex method.This is especially evident with the N-demethylation of 1,2,2,6,6-pentamethylpiperidine.Generally with dehydrogenations offering a possibility of generating a tertiary or a secondary carbenium ion, the latter alternative is mostly also realized to a minor extent.

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