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(Z)-hex-3-enyl acetoacetate, with the molecular formula C10H16O3, is an organic compound belonging to the acetoacetate class. It features a hexenyl group attached to an acetoacetate functional group, known for its aromatic properties that contribute to its diverse applications.

84434-20-8

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84434-20-8 Usage

Uses

Used in Food Industry:
(Z)-hex-3-enyl acetoacetate is used as a flavoring agent and aroma compound for imparting fruity and tropical flavors to various food products.
Used in Perfume and Fragrance Industry:
(Z)-hex-3-enyl acetoacetate is used as a key ingredient in the synthesis of perfumes and fragrances, enhancing their aromatic profiles.
Used in Chemical Synthesis:
(Z)-hex-3-enyl acetoacetate is utilized in the manufacture of other chemical compounds, showcasing its versatility in chemical reactions.
Used in Pharmaceutical Industry:
(Z)-hex-3-enyl acetoacetate is used for its potential applications in the pharmaceutical sector, likely due to its aromatic properties that could be beneficial in drug formulations.
Used in Cosmetic Industry:
(Z)-hex-3-enyl acetoacetate is employed in the cosmetic industry, possibly for its scent or as a component in the creation of cosmetic products.

Check Digit Verification of cas no

The CAS Registry Mumber 84434-20-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,3 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 84434-20:
(7*8)+(6*4)+(5*4)+(4*3)+(3*4)+(2*2)+(1*0)=128
128 % 10 = 8
So 84434-20-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O3/c1-3-4-5-6-7-13-10(12)8-9(2)11/h4-5H,3,6-8H2,1-2H3/b5-4-

84434-20-8SDS

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 Butanoic acid, 3-oxo-, (3Z)-3-hexenyl ester

1.2 Other means of identification

Product number -
Other names cis-3-Hexenyl acetoacetate

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:84434-20-8 SDS

84434-20-8Downstream Products

84434-20-8Relevant academic research and scientific papers

Sustainable transesterification of β-ketoesters catalyzed by amine grafted on silica gel

Hagiwara, Hisahiro,Koseki, Aiko,Isobe, Kohei,Shimizu, Ken-Ichi,Hoshi, Takashi,Suzuki, Toshio

, p. 2188 - 2190 (2004)

Transesterification of β-ketoesters with various alcohols has been effected by N,N-diethylaminopropylated silica gel (NDEAP) as a catalyst in refluxing xylene. Generality of the reaction was demonstrated by successful transesterification of olefinic alcohols, tertiary alcohols and alcohols having acid- or base-sensitive substituents. The catalyst has been efficiently recycled more than five times without any re-activation.

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