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83710-61-6

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83710-61-6 Usage

General Description

Naphthalene, 1-bromo-7-methoxy- is a chemical compound with the molecular formula C11H9BrO. It is a derivative of naphthalene, a polycyclic aromatic hydrocarbon. The compound is characterized by the presence of a bromine atom and a methoxy group on the naphthalene ring. It is commonly used in organic chemical synthesis and as a building block for the production of various pharmaceuticals and other organic compounds. Naphthalene, 1-bromo-7-methoxy- is important in the field of organic chemistry due to its reactivity and potential for forming diverse chemical structures. However, it is important to handle and use this compound with caution, as it may pose health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 83710-61-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,1 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83710-61:
(7*8)+(6*3)+(5*7)+(4*1)+(3*0)+(2*6)+(1*1)=126
126 % 10 = 6
So 83710-61-6 is a valid CAS Registry Number.

83710-61-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-7-methoxy-naphthalene

1.2 Other means of identification

Product number -
Other names 9-AZABICYCLO[3.3.1]NONAN-3-AMINE, 140-METHYL-

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:83710-61-6 SDS

83710-61-6Relevant 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.).

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