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135734-04-2

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135734-04-2 Usage

Chemical structure

A naphthalene ring with a methyl group at the 8-position and a methoxymethyl group at the 1-position.

Molecular weight

Approximately 190 g/mol

Appearance

Colorless to pale yellow liquid or solid

Solubility

Soluble in organic solvents, slightly soluble in water

Boiling point

Approximately 285-290°C

Melting point

Approximately -35°C

Density

Approximately 1.05 g/cm3

Flash point

Not available, but it is a flammable liquid

Odor

Sweet, floral, and powdery scent

Uses

Fragrance ingredient in household and personal care products
Perfumes, soaps, and detergents
Flavoring agent in food products
Additive in cosmetic formulations

Potential properties

Antimicrobial properties
Antioxidant properties

Industrial and commercial applications

Versatile compound with various applications in the fragrance, flavor, and cosmetic industries

Safety

May cause skin and eye irritation; avoid inhalation and ingestion; use proper protective equipment and ventilation during handling

Environmental impact

Not extensively studied, but due to its use in various products, it may contribute to environmental pollution if not properly managed or disposed of.

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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