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Ethyl 2,2-diphenylhexanoate is an organic compound with the chemical formula C20H24O2. It is a colorless to pale yellow liquid with a fruity, floral, and slightly woody odor. This ester is formed by the reaction of ethyl alcohol and 2,2-diphenylhexanoic acid, and it is commonly used as a fragrance ingredient in various cosmetic and personal care products due to its pleasant scent. It is also known for its ability to enhance the aroma of other fragrances, making it a valuable component in the perfumery industry. Ethyl 2,2-diphenylhexanoate is generally considered to be safe for use in these applications, but like any chemical, it should be handled with care to avoid potential skin or eye irritation.

2888-12-2

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2888-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2888-12-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,8 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2888-12:
(6*2)+(5*8)+(4*8)+(3*8)+(2*1)+(1*2)=112
112 % 10 = 2
So 2888-12-2 is a valid CAS Registry Number.

2888-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2,2-diphenylhexanoate

1.2 Other means of identification

Product number -
Other names 2,2-Diphenyl-hexansaeure-aethylester

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:2888-12-2 SDS

2888-12-2Upstream product

2888-12-2Relevant academic research and scientific papers

REACTIVITY OF CARBANIONS. XVI. ALKYLATION OF ALKALI-METAL SALTS OF CH ACIDS WITH ELECTRON WITHDRAWING SUBSTITUENTS BY BUTYL BROMIDE

Solov'yanov, A. A.,Beletskaya, I. P.,Reutov, O. A.

, p. 1608 - 1611 (2007/10/02)

The rate constants for the reaction of the free carbanions and ion pairs were determined in the alkylation of lithium and cesium salts of phenylacetonitrile, ethyl diphenylacetate, ethyl phenylacetate, and bis(pentafluorophenyl)methane by butyl bromide in dimethoxyethane at 25 gradC.The reactivity of the carbanions increases with their conjugate CH acids in the following order: ethyl diphenylacetate (0.78 liter/mole.sec) bis(pentafluorophenyl)methane (2.7 liter/mole.sec) phenylacetonitrile (6.9 liter/mole.sec) ethyl phenylacetate (9.5 liter/mole.sec).

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