Welcome to LookChem.com Sign In|Join Free

CAS

  • or

109962-21-2

Post Buying Request

109962-21-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

109962-21-2 Usage

Chlorinated derivative

1-methylnaphthalene

Common uses

Production of dyes, pigments, and other organic compounds

Physical state

Clear to slightly yellow liquid

Odor

Faint, aromatic

Solubility

Sparingly soluble in water, soluble in organic solvents

Toxicity

Moderate acute toxicity, potential occupational hazard

Health and environmental effects

Harmful effects on human health and the environment

Check Digit Verification of cas no

The CAS Registry Mumber 109962-21-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,9,6 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 109962-21:
(8*1)+(7*0)+(6*9)+(5*9)+(4*6)+(3*2)+(2*2)+(1*1)=142
142 % 10 = 2
So 109962-21-2 is a valid CAS Registry Number.

109962-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-5-methylnaphthalene

1.2 Other means of identification

Product number -
Other names 1-Chlor-5-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:109962-21-2 SDS

109962-21-2Downstream Products

109962-21-2Relevant articles and documents

A Visible Light and Iron-mediated Carbocationic Route to Polysubstituted 1-Halonaphthalenes by Benzannulation using Allylbenzenes and Polyhalomethanes

Roslan, Irwan Iskandar,Zhang, Hongwei,Ng, Kian-Hong,Jaenicke, Stephan,Chuah, Gaik-Khuan

, p. 1007 - 1013 (2020/12/30)

A wide array of polysubstituted 1-bromo and chloronaphthalenes are obtained from coupling of allylbenzenes and polyhalomethanes. The reaction is mediated by iron metal under visible light irradiation and proceeds via a Kharasch addition intermediate followed by intramolecular FeIII mediated Friedel-Crafts alkylation, with the formation of two Csp2?Csp2 bonds in the process. This method gives easy access to 1-halonaphthalenes with substituent(s) at C-5 to C-8 that are otherwise hard to synthesize. (Figure presented.).

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 109962-21-2