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4342-60-3

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4342-60-3 Usage

Description

4-METHYL-3-CYCLOHEXENE-1-CARBOXYLIC ACID is an organic compound with the chemical formula C8H12O2. It is characterized by a cyclohexene ring with a methyl group at the 4-position and a carboxylic acid group at the 1-position. This molecule is known for its unique chemical properties and potential applications in various industries.

Uses

Used in Perfumery Industry:
4-METHYL-3-CYCLOHEXENE-1-CARBOXYLIC ACID is used as a fragrance ingredient for its ability to mimic the scent of cumin oil and/or cumene aldehyde. It is particularly suitable for use in perfumes that are applied to fabric softeners, cleaning compounds, shampoos, and other personal care products.
Used in Cleaning Compounds:
In the cleaning industry, 4-METHYL-3-CYCLOHEXENE-1-CARBOXYLIC ACID serves as a replacement for cumin oil and/or cumene aldehyde, providing a pleasant scent to cleaning products without the need for more expensive or less stable ingredients.
Used in Fabric Softeners:
4-METHYL-3-CYCLOHEXENE-1-CARBOXYLIC ACID is used as a scent enhancer in fabric softeners, imparting a fresh and appealing fragrance to laundered fabrics.
Used in Shampoos:
In the personal care industry, 4-METHYL-3-CYCLOHEXENE-1-CARBOXYLIC ACID is used in shampoos to provide a pleasant scent and improve the overall sensory experience of hair washing.
Used in Aromatherapy:
4-METHYL-3-CYCLOHEXENE-1-CARBOXYLIC ACID may also find use in aromatherapy products, where its unique scent can contribute to creating a relaxing or invigorating atmosphere.

Check Digit Verification of cas no

The CAS Registry Mumber 4342-60-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,4 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4342-60:
(6*4)+(5*3)+(4*4)+(3*2)+(2*6)+(1*0)=73
73 % 10 = 3
So 4342-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O2/c1-6-2-4-7(5-3-6)8(9)10/h2,7H,3-5H2,1H3,(H,9,10)

4342-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylcyclohex-3-ene-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-methyl-3-cyclohexene carboxylic 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:4342-60-3 SDS

4342-60-3Relevant articles and documents

TWO CONVENIENT METHODS FOR THE GENERATION OF "METHYLENE MELDRUM'S ACID" FOR DIELS- ALDER REACTIONS.

Buzinkai, John F.,Hrubowchak, David M.,Smith, Francis X.

, p. 3195 - 3198 (1985)

The transient isopropylidene methylenemalonate can be easily generated by treating either Meldrum's acid or diisopropylidene methylenedimalonate with formaldehyde, and trapped by reactive dienes.

BORON-BASED CYCLOADDITION CATALYSTS AND METHODS FOR THE PRODUCTION OF BIO-BASED TEREPHTHALIC ACID, ISOPHTHALIC ACID AND POLY (ETHYLENE TEREPHTHALATE)

-

Paragraph 00172; 00173, (2017/04/11)

Methods for producing cycloaddition products comprising: reacting a diene with a dienophile in the presence of one or more boron-based catalysts of Formula I or Formula II are provided. In particular, the methods can be used to prepare 4-methyl-3-cyclohexene- 1-carboxylic acid and 3-methyl-3-cyclohexene-l-carboxylic acid, including bio-based versions thereof. The cycloaddition products can be advantageously used in the production of terephthalic acid and isophthalic acid, and ultimately, poly(ethylene terephthalate), and bio-based versions thereof. Formula I Formula II

Polyelectrolyte-catalyzed Diels–Alder reactions

Pothanagandhi, Nellepalli,Sivaramakrishna, Akella,Vijayakrishna, Kari

, p. 132 - 136 (2016/08/05)

Imidazolium-based poly(ionic liquids) bearing bromide and bis(trifluoromethane)sulfonimide as counteranions [poly(ViEIm)Br and poly(ViEIm)NTf2] derived from reversible addition fragmentation chain transfer (RAFT) polymerization techniques are u

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