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135734-04-2

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135734-04-2 Usage

General Description

1-(MethoxyMethyl)-8-Methylnaphthalene is a chemical compound consisting of a naphthalene ring with a methyl group at the 8-position and a methoxymethyl group at the 1-position. It is commonly used as a fragrance ingredient in various household and personal care products. This chemical is known for its sweet, floral, and powdery scent and is often used in perfumes, soaps, and detergents. It is also used as a flavoring agent in food products and as an additive in cosmetic formulations. Additionally, 1-(MethoxyMethyl)-8-Methylnaphthalene has been studied for its potential antimicrobial and antioxidant properties, making it a versatile compound with various industrial and commercial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 135734-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,7,3 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 135734-04:
(8*1)+(7*3)+(6*5)+(5*7)+(4*3)+(3*4)+(2*0)+(1*4)=122
122 % 10 = 2
So 135734-04-2 is a valid CAS Registry Number.

135734-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Methoxymethyl)-8-methylnaphthalene

1.2 Other means of identification

Product number -
Other names -

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:135734-04-2 SDS

135734-04-2Downstream Products

135734-04-2Relevant articles and documents

A carbene to biradical rearrangement: Reaction paths from (8-methyl-1-naphthyl)carbene to acenaphthene

Biewer, Michael C.,Platz, Matthew S.,Roth, Martin,Wirz, Jakob

, p. 8069 - 8073 (2007/10/02)

Photochemical nitrogen elimination from 1-(diazomethyl)-8-methylnaphthalene (2) yields acenaphthene (3) via the reactive intermediates (8-methyl-1-naphthyl)carbene (a) and 1,8-naphthoquinodimethane (b). The triplet biradical b was observed by absorption s

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