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34185-71-2

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34185-71-2 Usage

Description

4-Hexenoic acid, 6-(1,4-dihydro-3-methyl-1,4-dioxo-2-naphthalenyl)-4-methyl-, (E)is a complex chemical compound that features a long-chain unsaturated fatty acid structure with six carbon atoms and a double bond at the sixth position. Characterized by a 1,4-dihydro-3-methyl-1,4-dioxo-2-naphthalenyl group and a methyl group attached to the fourth and sixth carbon atoms, respectively, the (E)prefix denotes the trans configuration of the double bond. 4-Hexenoic acid,
6-(1,4-dihydro-3-methyl-1,4-dioxo-2-naphthalenyl)-4-methyl-, (E)is known for its unique and versatile chemical properties, making it suitable for a range of applications.

Uses

Used in Food Additives Industry:
4-Hexenoic acid, 6-(1,4-dihydro-3-methyl-1,4-dioxo-2-naphthalenyl)-4-methyl-, (E)is used as a flavoring agent for enhancing the taste and aroma of various food products. Its unique chemical structure contributes to the development of distinct flavor profiles, adding value to the final product.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 4-Hexenoic acid, 6-(1,4-dihydro-3-methyl-1,4-dioxo-2-naphthalenyl)-4-methyl-, (E)serves as an active pharmaceutical ingredient or an intermediate in the synthesis of drugs. Its versatile chemical properties allow for the development of medications with specific therapeutic effects, addressing various health conditions.
Used in Fragrance Industry:
4-Hexenoic acid, 6-(1,4-dihydro-3-methyl-1,4-dioxo-2-naphthalenyl)-4-methyl-, (E)is utilized as a fragrance ingredient in the creation of perfumes, colognes, and other scented products. Its distinct chemical composition contributes to the formation of unique and appealing scents, enhancing the sensory experience of consumers.

Check Digit Verification of cas no

The CAS Registry Mumber 34185-71-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,8 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34185-71:
(7*3)+(6*4)+(5*1)+(4*8)+(3*5)+(2*7)+(1*1)=112
112 % 10 = 2
So 34185-71-2 is a valid CAS Registry Number.

34185-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-2-methyl-3-(5′-carboxy-3′-methylpent-2′-enyl)-1,4-naphthoquinone

1.2 Other means of identification

Product number -
Other names (E)-4-Methyl-6-(3-methyl-1,4-dioxo-1,4-dihydro-naphthalen-2-yl)-hex-4-enoic acid

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:34185-71-2 SDS

34185-71-2Downstream Products

34185-71-2Relevant articles and documents

Efficient Syntheses of Vitamin K Chain-Shortened Acid Metabolites

Teitelbaum, Aaron M.,Scian, Michele,Nelson, Wendel L.,Rettie, Allan E.

, p. 944 - 948 (2015)

Vitamin K sequentially undergoes ω-oxidation followed by successive rounds of β-oxidation to ultimately produce two chain-shortened carboxylic acid metabolites, vitamin K acid 1 and vitamin K acid 2. Two facile syntheses of these acid metabolites are desc

Regio- and stereoselective terminal allylic carboxymethylation of gem-dimethyl olefins. Synthesis of biologically important linear degraded terpenoids

Masaki,Sakuma,Kaji

, p. 1930 - 1940 (2007/10/02)

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Ubiquinone and related compounds. XXVII. Synthesis of urinary metabolites of phylloquinone and α tocopherol

Watanabe,Kawada,Nishikawa,Imada,Morimoto

, p. 566 - 575 (2007/10/08)

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