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3-Ethyl-o-cresol is a chemical compound belonging to the cresol family, characterized by a distinctive phenolic odor. It is a derivative of o-cresol with an additional ethyl group attached to the benzene ring, commonly utilized for its fragrance properties and antimicrobial capabilities.

1123-73-5

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1123-73-5 Usage

Uses

Used in Fragrance Industry:
3-Ethyl-o-cresol is used as a fragrance ingredient for its aromatic properties in various consumer products such as perfumes, soaps, and cosmetics, enhancing their scent profiles.
Used in Personal Care Industry:
3-Ethyl-o-cresol is used as an antimicrobial agent in personal care products to prevent the growth of harmful microorganisms, ensuring product safety and efficacy.
Used in Cleaning Products Industry:
3-Ethyl-o-cresol is used as a preservative and antimicrobial agent in cleaning products to maintain cleanliness and prevent microbial contamination.
However, due to its potential to cause skin, eye, and respiratory irritation, as well as allergic reactions in some individuals, it is crucial to handle 3-ethyl-o-cresol with care and adhere to safety guidelines during its use.

Check Digit Verification of cas no

The CAS Registry Mumber 1123-73-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1123-73:
(6*1)+(5*1)+(4*2)+(3*3)+(2*7)+(1*3)=45
45 % 10 = 5
So 1123-73-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O/c1-3-8-5-4-6-9(10)7(8)2/h4-6,10H,3H2,1-2H3

1123-73-5SDS

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 3-ethyl-2-methylphenol

1.2 Other means of identification

Product number -
Other names 3-Aethyl-2-methyl-phenol

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:1123-73-5 SDS

1123-73-5Relevant academic research and scientific papers

Synthesis of Highly Substituted Phenols and Benzenes with Complete Regiochemical Control

Zhang, Xiaojie,Beaudry, Christopher M.

supporting information, p. 6086 - 6090 (2020/08/12)

Substituted phenols are requisite molecules for human health, agriculture, and diverse synthetic materials. We report a chemical synthesis of phenols, including penta-substituted phenols, that accommodates programmable substitution at any position. This method uses a one-step conversion of readily available hydroxypyrone and nitroalkene starting materials to give phenols with complete regiochemical control and in high chemical yield. Additionally, the phenols can be converted into highly and even fully substituted benzenes.

Synthesis of aromatic compounds using combinations of ring-closing olefin metathesis, dehydration, oxidation, and tautomerization

Yoshida, Kazuhiro,Toyoshima, Takeharu,Imamoto, Tsuneo

scheme or table, p. 1512 - 1517 (2009/05/06)

An approach to aromatic compounds using combinations of ring-closing olefin metathesis (RCM), dehydration, oxidation, and tautomerization is reported. The RCM reaction of l,7-diene-3,5-diols, which were readily prepared by the allylation of aldol products, gave corresponding cyclized products, 4-cyclohexene-l,3-diols, in high yields. The subsequent dehydration or oxidation of 4-cyclohexene-1,3-diols led to versatile substituted benzenes including phenol and resorcinol derivatives.

Efficient synthetic routes to aromatic compounds using ring-closing olefin metathesis followed by dehydration, oxidation, and tautomerization

Yoshida, Kazuhiro,Toyoshima, Takeharu,Imamoto, Tsuneo

, p. 3774 - 3776 (2008/03/12)

A simple synthetic approach to aromatic compounds using combinations of RCM, dehydration, oxidation, and tautomerization is described. The Royal Society of Chemistry.

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