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82898-13-3

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82898-13-3 Usage

Structure

Six-carbon chain with a carboxylic acid group and a double bond at the fourth position

Appearance

Colorless to pale yellow liquid

Odor

Fruity, green, and fatty

Uses

Production of flavors and fragrances for perfumes, soaps, and food products

Biological activities

Potential antifungal and antimicrobial properties, of interest in pharmaceutical research

Check Digit Verification of cas no

The CAS Registry Mumber 82898-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,9 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82898-13:
(7*8)+(6*2)+(5*8)+(4*9)+(3*8)+(2*1)+(1*3)=173
173 % 10 = 3
So 82898-13-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O2/c1-6(2)4-5-7(3)8(9)10/h4,7H,5H2,1-3H3,(H,9,10)

82898-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dimethylhex-4-enoic acid

1.2 Other means of identification

Product number -
Other names Methyl-<3,3-dimethyl-allyl>-essigsaeure

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:82898-13-3 SDS

82898-13-3Downstream Products

82898-13-3Relevant articles and documents

Indium-mediated Reformatsky-Claisen rearrangement

Ishihara, Jun,Watanabe, Yuki,Koyama, Noriko,Nishino, Yukihiro,Takahashi, Keisuke,Hatakeyama, Susumi

experimental part, p. 3659 - 3667 (2011/06/21)

A new variant of the Reformatsky-Claisen rearrangement is described. The reaction of substituted allyl α-bromoacetates with indium and indium(III) chloride under ultrasonication provides a general entry into the functionalized synthon.

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