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6698-70-0

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6698-70-0 Usage

Description

1-(4-METHYLPHENOXY)-2-PROPANONE, also known as 1-(4-Methylphenoxy)-2-propanone, is a chemical compound characterized by its molecular formula C10H12O2. It is a clear, colorless liquid with a faint odor and is insoluble in water but soluble in organic solvents. 1-(4-METHYLPHENOXY)-2-PROPANONE is recognized for its use in the fragrance and flavor industry, as well as its application as a solvent in various industrial and commercial processes. However, it is essential to handle 1-(4-METHYLPHENOXY)-2-PROPANONE with care due to its potential as a skin irritant, and proper safety precautions should be followed.

Uses

Used in Fragrance and Flavor Industry:
1-(4-METHYLPHENOXY)-2-PROPANONE is used as a fragrance ingredient for its ability to enhance the scent of various products. It contributes to the creation of distinct and appealing aromas in the fragrance industry.
Used in Flavor Production:
In the flavor industry, 1-(4-METHYLPHENOXY)-2-PROPANONE is utilized to impart specific taste profiles to different products, making it a valuable component in the development of unique flavors.
Used as a Solvent in Industrial Applications:
1-(4-METHYLPHENOXY)-2-PROPANONE serves as a solvent in various industrial processes, where its solubility in organic solvents makes it a suitable candidate for dissolving substances and facilitating chemical reactions.
Used as a Solvent in Commercial Applications:
Similarly, in commercial applications, 1-(4-METHYLPHENOXY)-2-PROPANONE is employed as a solvent for its capacity to dissolve and interact with other compounds, making it a versatile component in the production of various products.

Check Digit Verification of cas no

The CAS Registry Mumber 6698-70-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,9 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6698-70:
(6*6)+(5*6)+(4*9)+(3*8)+(2*7)+(1*0)=140
140 % 10 = 0
So 6698-70-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O2/c1-8-3-5-10(6-4-8)12-7-9(2)11/h3-6H,7H2,1-2H3

6698-70-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methylphenoxy)propan-2-one

1.2 Other means of identification

Product number -
Other names p-Tolyloxy-aceton

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:6698-70-0 SDS

6698-70-0Relevant articles and documents

Selective Cross-Dehydrogenative C(sp3)-H Arylation with Arenes

Hao, Hong-Yan,Mao, Yang-Jie,Xu, Zhen-Yuan,Lou, Shao-Jie,Xu, Dan-Qian

supporting information, p. 2396 - 2402 (2020/03/13)

Selective C(sp3)-C(sp2) bond construction is of central interest in chemical synthesis. Despite the success of classic cross-coupling reactions, the cross-dehydrogenative coupling between inert C(sp3)-H and C(sp2)-H bonds represents an attractive alternative toward new C(sp3)-C(sp2) bonds. Herein, we establish a selective inter-and intramolecular C(sp3)-H arylation of alcohols with nondirected arenes that thereby provides a general pathway to access a wide range of β-arylated alcohols, including tetrahydronaphthalen-2-ols and benzopyran-3-ols, with high to excellent chemo-and regioselectivity.

Wacker oxidation of terminal olefins in a mixture of [bmim][BF4] and water

Ansari,Joyasawal, Sipak,Gupta, Manoj K.,Yadav,Gree

, p. 7507 - 7510 (2007/10/03)

A simple and efficient PdCl2/CuCl catalyzed oxidation of alkenes has been successfully developed using a mixture of water and the ionic liquid [bmim][BF4] as solvent. Starting from various types of terminal olefins, the corresponding ketones have been prepared under mild reaction conditions and obtained in good to excellent yields after a simple extraction with diethyl ether. Furthermore, it was possible to recycle and reuse the ionic liquid and the catalytic system.

POLYMER-SUPPORTED REAGENTS: AN EFFICIENT METHOD FOR THE SYNTHESIS OF PHENOXYACETONES

Salunkhe, Deepak,Jagdale, Mansingrao,Mane, Ramchandra,Salunkhe, Manikrao

, p. 411 - 412 (2007/10/02)

Phenoxides supported on Amberlite IRA-400 reacted with chloroacetone to give the corresponding phenoxyacetones in high yields and purity.

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