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1-(3,8,8-trimethyl-5,6,7,8-tetrahydronaphthalen-2-yl)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87756-40-9

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87756-40-9 Usage

Molecular Structure

Complex, consisting of a tetrahydronaphthalene core with methyl groups at positions 3, 8, and 8

Industry Usage

Fragrance industry

Scent

Musky, sweet, and floral

Function

Used as a fixative in perfumes

Source

Derived from natural sources (plants and animals) and synthesized in laboratories

Applications

Personal care products, household items, and industrial applications

Stability

Stable, making it suitable for various applications

Safety Precautions

Handle with care and in accordance with regulations to avoid potential risks

Check Digit Verification of cas no

The CAS Registry Mumber 87756-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,5 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87756-40:
(7*8)+(6*7)+(5*7)+(4*5)+(3*6)+(2*4)+(1*0)=179
179 % 10 = 9
So 87756-40-9 is a valid CAS Registry Number.

87756-40-9SDS

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 1-(3,8,8-trimethyl-6,7-dihydro-5H-naphthalen-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-(5,6,7,8-tetrahydro-3,8,8-trimethyl-2-naphthalenyl)ethanone

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:87756-40-9 SDS

87756-40-9Relevant academic research and scientific papers

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.

Selective syntheses of substituted 6-alkyl-1,1-dimethyl-1,2,3,4-tetrahydronaphthalenes

Parlow, John J.

, p. 2577 - 2588 (2007/10/02)

β-ionone is cyclized to 1,1,6-trimethyl-1,2,3,4-tetrahydronaphthalene in 80-95% yield. Selective derivatization at the 5- and/or 7-positions of 6-alkyl-1,1-dimethyl-1,2,3,4-tetrahydronaphthalenes was achieved by nitration, acylation, and reduction.

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