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6335-36-0

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6335-36-0 Usage

General Description

1-(2,4,6-trimethyl-3-propanoyl-phenyl)propan-1-one, also known as 3'-oxo-alpha,alpha,alpha-trimethylacetophenone, is a chemical compound with the molecular formula C14H18O. It is a white crystalline solid with a sweet, fruity odor and is commonly used in the fragrance industry as a flavoring agent in perfumes and cosmetics. It is also used in the production of various pharmaceuticals and as a synthetic intermediate in organic chemistry. 1-(2,4,6-trimethyl-3-propanoyl-phenyl)propan-1-one is known for its low toxicity and is generally regarded as safe for use in consumer products. However, it should be handled and stored with care to avoid any potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 6335-36-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6335-36:
(6*6)+(5*3)+(4*3)+(3*5)+(2*3)+(1*6)=90
90 % 10 = 0
So 6335-36-0 is a valid CAS Registry Number.

6335-36-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-Trimethyl-2,4-dipropionyl-benzol

1.2 Other means of identification

Product number -
Other names 21.41-Dioxo-1.3.5-trimethyl-2.4-dipropyl-benzol

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:6335-36-0 SDS

6335-36-0Relevant articles and documents

A Novel Friedel-Crafts Reaction of Hindered Ketones

Roberts, Royston M.,El-Khawaga, Ahmed M.,Roengsumran, Sophon

, p. 3180 - 3183 (2007/10/02)

Mesitylene has been shown to react with acetyl chloride in the presence of aluminium chloride to form 1,1-dimesitylethene.Acetomesitylene has been demonstrated to be an intermediate in the reaction, which proceeds in the second step by nucleophilic attack by the arene on the carbonyl group of acetomesitylene, which is activated by the formation of a polarized complex with aluminum chloride.Mesitylene reacts similarly with propionyl chloride, forming 1,1-dimesitylpropene; propiomesitylene is an intermediate.Steric and electronic factors responsible for this unique Friedel-Crafts reaction are discussed.

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