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3-Cyclohexene-1-carboxylic acid, 4-(1-methylethyl)-, also known as 1,2,5,6-Tetrahydrocuminic acid, is an organic compound found in cumin oil. It has a cuminic, sweaty odor and is characterized by its cyclohexene ring and carboxylic acid functional group.

71298-42-5

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71298-42-5 Usage

Uses

Used in Flavor and Fragrance Industry:
3-Cyclohexene-1-carboxylic acid, 4-(1-methylethyl)is used as a flavoring agent for its characteristic cuminic, sweaty odor. It adds a unique aroma to various food products and beverages, enhancing their taste and appeal.
Used in Perfumery:
3-Cyclohexene-1-carboxylic acid, 4-(1-methylethyl)is used as a fragrance ingredient in the perfumery industry. Its distinct odor profile makes it suitable for creating complex and long-lasting scents in perfumes, colognes, and other fragrance products.
Used in Chemical Synthesis:
3-Cyclohexene-1-carboxylic acid, 4-(1-methylethyl)can be used as a building block in the synthesis of various organic compounds. Its cyclohexene ring and carboxylic acid functional group make it a versatile intermediate for the production of pharmaceuticals, agrochemicals, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 71298-42-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,2,9 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71298-42:
(7*7)+(6*1)+(5*2)+(4*9)+(3*8)+(2*4)+(1*2)=135
135 % 10 = 5
So 71298-42-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O2/c1-7(2)8-3-5-9(6-4-8)10(11)12/h3,7,9H,4-6H2,1-2H3,(H,11,12)

71298-42-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name p-menth-3-en-7-oic acid

1.2 Other means of identification

Product number -
Other names p-Menth-3-en-7-saeure

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:71298-42-5 SDS

71298-42-5Relevant academic research and scientific papers

Substrate specific silver(I)-catalyzed cycloisomerization of diene involving alkyl rearrangements: Syntheses of 1,2,5,6-tetrahydrocuminic acid, p-menth-3-en-7-ol, and p-menth-3-en-7-al

Inagaki, Fuyuhiko,Matsumoto, Mizuki,Hira, Shisen,Mukai, Chisato

, p. 822 - 825 (2017/09/12)

The novel cationic Ag(I)-catalyzed cycloisomerization, which is associated with alkyl rearrangements, from dimethyl 2-allyl-2-prenylmalonate (1) to dimethyl 4-isopropylcyclohex-3-ene-1,1-dicarboxylate (2) has been developed. Derivatization from the dieste

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