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6079-97-6

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6079-97-6 Usage

General Description

2-ethylhexyl acetoacetate, also known as acetoacetic acid 2-ethylhexyl ester, is a chemical compound commonly used as a fragrance ingredient and flavoring additive. It is a colorless liquid with a fruity odor, and is soluble in alcohol and oils but insoluble in water. This chemical is commonly used in the production of perfumes, soaps, and other personal care products, as well as in the food and beverage industry as a flavor enhancer. 2-ethylhexyl acetoacetate is also used as a solvent for various polymers and in the manufacture of resins and coatings. Overall, this chemical plays a significant role in various industries as a fragrance and flavoring agent, as well as a solvent component in several applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6079-97-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,7 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6079-97:
(6*6)+(5*0)+(4*7)+(3*9)+(2*9)+(1*7)=116
116 % 10 = 6
So 6079-97-6 is a valid CAS Registry Number.
InChI:InChI=1/C32H20F9NO6/c1-12-6-23(44)26-21(27(12)45)11-19-17(24(26)20-10-16(2-5-22(20)43)48-32(39,40)41)3-4-18-25(19)29(47)42(28(18)46)15-8-13(30(33,34)35)7-14(9-15)31(36,37)38/h2-3,5-10,18-19,24-25,43H,4,11H2,1H3

6079-97-6SDS

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 2-ethylhexyl 3-oxobutanoate

1.2 Other means of identification

Product number -
Other names EINECS 228-018-6

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:6079-97-6 SDS

6079-97-6Downstream Products

6079-97-6Relevant articles and documents

An efficient synthesis of β-ketoesters via transesterification and its application in Biginelli reaction under solvent-free, catalyst-free conditions

Dharma Rao,Acharya,Kaushik

supporting information, p. 6644 - 6647 (2013/11/19)

A simple and efficient transesterification process for the synthesis of β-ketoester derivatives has been achieved by the reaction of methyl β-ketoester with higher alcohols at 110 C under solvent-free, catalyst-free conditions and its application in synthesis of 3,4-dihydropyrimidin-2(1H)-ones C-5 ester derivatives via Biginelli reaction has been described.

Method of preparing β-amino derivatives of α,β-unsaturated esters

-

, (2008/06/13)

A method for the preparation of β-amino derivatives of α,β-unsaturated esters of the formula CH3 C(NH2)=CHCOOR' where R' is C1 to C10 linear or branched alkyl or substituted C1 to C10 linear or branched alkyl. A reaction mixture of an acetoacetate ester of the formula CH3 C(O)CH2 C(O)OR' wherein R' is the same as defined above is first formed in an organic solvent and this mixture reacted with aqueous ammonium hydroxide in the presence of a salt of ammonia or of a metal selected from the group consisting of lithium, zinc, cadmium, cerium and lead. The salt is soluble in the organic solvent to an extent sufficient to catalyze the reaction between ammonia and the ester.

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