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2,3-Dimethyl-4-pentenal is an organic compound with the chemical formula C7H12O. It is a colorless liquid with a strong, pungent odor and is classified as an aldehyde. 2,3-Dimethyl-4-pentenal is characterized by the presence of two methyl groups (CH3) at the 2nd and 3rd carbon atoms, and a carbon-carbon double bond between the 4th and 5th carbon atoms. It is commonly used as a flavoring agent and fragrance component in the food and perfume industries, contributing to the aroma of fruits, vegetables, and floral scents. Due to its reactive nature, 2,3-dimethyl-4-pentenal can undergo various chemical reactions, such as oxidation and reduction, making it a versatile building block in organic synthesis.

5714-71-6

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5714-71-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5714-71-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,1 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5714-71:
(6*5)+(5*7)+(4*1)+(3*4)+(2*7)+(1*1)=96
96 % 10 = 6
So 5714-71-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O/c1-4-6(2)7(3)5-8/h4-7H,1H2,2-3H3

5714-71-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dimethylpent-4-enal

1.2 Other means of identification

Product number -
Other names 2,3-dimethyl-pent-4-enal

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:5714-71-6 SDS

5714-71-6Downstream Products

5714-71-6Relevant academic research and scientific papers

PALLADIUM(II)-CATALYZED CLAISEN REARRANGEMENT OF ALLYL VINYL ETHERS

Baan, J. L. van der,Bickelhaupt, F.

, p. 6267 - 6270 (2007/10/02)

The Claisen rearrangement of allyl vinyl ethers is catalyzed by PdCl2(CH3CN)2, provided that alkyl substituents protect the vinyl ether double bond from coordination by the metal catalyst.

Method for the preparation of 2,3-dimethyl-pent-4en-aldehyde

-

, (2008/06/13)

A process for the production of 2-methyl-2-sec. butyl-1,3-propanediol from crotyl alcohol is disclosed. The diol obtained is useful in the manufacture of 2-methyl-2-(1-methylpropyl)-1,3-propanediol dicarbamate a valuable antihypertensive agent.

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