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27413-60-1

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27413-60-1 Usage

Category

Organic compound

Subgroup

Ketone derivative

Family

Naphtalene family

Usage

a. Perfumes and fragrances manufacturing
b. Synthesis of other organic compounds in the chemical industry

Aromatic Properties

Used for its aromatic properties in the perfume industry

Molecular Structure

a. Naphtalene ring
b. Ethyl substituent
c. Dimethyl substituent
d. Carbonyl group attached to the naphthalene ring

Distinctive Characteristics

Derived from the molecular structure and functional groups present in the compound

Check Digit Verification of cas no

The CAS Registry Mumber 27413-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,4,1 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27413-60:
(7*2)+(6*7)+(5*4)+(4*1)+(3*3)+(2*6)+(1*0)=101
101 % 10 = 1
So 27413-60-1 is a valid CAS Registry Number.

27413-60-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-ethyl-8,8-dimethyl-6,7-dihydro-5H-naphthalen-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1.1-Dimethyl-6-aethyl-7-acetyl-tetralin

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:27413-60-1 SDS

27413-60-1Downstream Products

27413-60-1Relevant articles and documents

Synthesis and Herbicidal Activity of Substituted Tetrahydronaphthalenes: I

Parlow, John J.,Mahoney, Martin D.

, p. 137 - 144 (2007/10/03)

This paper reports the synthesis and the biological activity of substituted 6-alkyl-1,2,3,4-tetrahydro-1,1-dimethylnaphthalenes in which the substituents at the 5- and/or 7-position are varied with a multitude of functional groups. These compounds exhibited pre-emergent herbicidal activity which was a function of the electron-withdrawing ability and the size of the groups substituted at the 5- and/or 7-position. Nitro and/or nitrile groups at these positions tended to optimize activity.

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