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Hexyl naphthalen-1-ylacetate is an organic compound with the chemical formula C18H22O2. It is a derivative of naphthalene, a polycyclic aromatic hydrocarbon, and is characterized by a naphthalen-1-yl group attached to an acetate group through an ester linkage. hexyl naphthalen-1-ylacetate is often used as a fragrance ingredient in various consumer products, such as perfumes, due to its pleasant, floral scent. It is also known for its ability to enhance the aroma of other fragrances when used in combination. The compound is typically synthesized through chemical reactions and is subject to safety regulations and guidelines to ensure its safe use in consumer products.

2876-73-5

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2876-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2876-73-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,7 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2876-73:
(6*2)+(5*8)+(4*7)+(3*6)+(2*7)+(1*3)=115
115 % 10 = 5
So 2876-73-5 is a valid CAS Registry Number.

2876-73-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Hexyl 1-naphthylacetate

1.2 Other means of identification

Product number -
Other names 8-Hydroxy-7-tetradecanone

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:2876-73-5 SDS

2876-73-5Downstream Products

2876-73-5Relevant academic research and scientific papers

Efficient and simple NaBH4 reduction of esters at cationic micellar surface

Das, Debapratim,Roy, Sangita,Das, Prasanta Kumar

, p. 4133 - 4136 (2007/10/03)

(Chemical Equation Presented) A simple, efficacious, and biocompatible methodology for reducing esters with sodium borohydride at an aqueous cationic micellar surface under ambient conditions has been developed. The present method holds promise for future use in selective functional group reduction and stereocontrolled alcohol synthesis.

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