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6039-60-7

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6039-60-7 Usage

Molecular weight

230.26 g/mol

Structure

The molecule consists of a naphthalene ring system with a carboxylic acid group (-COOH) at position 1 and a methoxy group (-OCH3) at position 8.

+ Appearance

White crystalline solid

+ Solubility

Slightly soluble in water, soluble in organic solvents like ethanol, methanol, and acetone.

+ Boiling point

292-294°C

+ Melting point

81-83°C

Uses

In the synthesis of various organic compounds and pharmaceuticals.

Safety precautions

Handle with care and follow proper safety precautions in a laboratory or industrial setting.

Check Digit Verification of cas no

The CAS Registry Mumber 6039-60-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,3 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6039-60:
(6*6)+(5*0)+(4*3)+(3*9)+(2*6)+(1*0)=87
87 % 10 = 7
So 6039-60-7 is a valid CAS Registry Number.

6039-60-7SDS

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 8-methoxy-[1]naphthoic acid methyl ester

1.2 Other means of identification

Product number -
Other names Methyl-8-methoxy-1-naphthoat

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:6039-60-7 SDS

6039-60-7Downstream Products

6039-60-7Relevant articles and documents

Facile alkoxyl exchange of 2-methoxybenzoates via nucleophilic aromatic substitution with sodium alkoxides in dimethylformamide

Hattori,Satoh,Miyano

, p. 3840 - 3842 (2007/10/02)

Methyl 2-methoxybenzoate undergoes facile nuclear-methoxyl displacement by treatment with sodium butexide or isopropoxide in dimethylformamide.

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