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6626-23-9

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6626-23-9 Usage

General Description

1-CHLOROMETHYL-2-METHYLNAPHTHALENE is a chemical compound belonging to the class of naphthalenes, which are aromatic hydrocarbons commonly used in the production of dyes, pesticides, and pharmaceuticals. 1-CHLOROMETHYL-2-METHYLNAPHTHALENE is a chlorinated derivative of 2-methylnaphthalene, containing a chlorine atom and a methyl group attached to the naphthalene ring. It is primarily used as an intermediate in the synthesis of other chemicals, and as a reagent in organic chemistry reactions. Its specific properties and applications may vary depending on its purity and the specific conditions of its use. 1-CHLOROMETHYL-2-METHYLNAPHTHALENE is considered potentially hazardous, and proper safety precautions should be taken when handling and using it.

Check Digit Verification of cas no

The CAS Registry Mumber 6626-23-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6626-23:
(6*6)+(5*6)+(4*2)+(3*6)+(2*2)+(1*3)=99
99 % 10 = 9
So 6626-23-9 is a valid CAS Registry Number.
InChI:InChI=1/C24H23FN2O4S/c1-5-31-24(30)19-15(4)20(22(29)26-18-10-9-13(2)11-14(18)3)32-23(19)27-21(28)16-7-6-8-17(25)12-16/h6-12H,5H2,1-4H3,(H,26,29)(H,27,28)

6626-23-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-CHLOROMETHYL-2-METHYLNAPHTHALENE

1.2 Other means of identification

Product number -
Other names 1-Chlormethyl-2-methyl-naphthalin

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:6626-23-9 SDS

6626-23-9Relevant articles and documents

Costakis et al.

, p. 3106,3111 (1974)

Pd-catalyzed C4-Dearomative Allylation of Benzyl Ammoniums with Allyltributylstannane

Kayashima, Yuki,Komatsuda, Masaaki,Muto, Kei,Yamaguchi, Junichiro

supporting information, p. 836 - 839 (2020/07/23)

A dearomative C4-allylation of benzyl ammoniums with allyltributylstannane by a palladium catalysis is described. A triarylphosphine-ligated palladium catalyst, which is capable of cleaving benzylic CN bonds, realized facile dearomative reactions with C4 selectivity. Combined with precedented C2- A nd C3-selective functionalizations of benzyl amine derivatives, the present reaction can provide a new synthetic option for the synthesis of multi-substituted alicyclic compounds as well as aromatic compounds.

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