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Phenol, 3,4,5-trimethyl-, acetate, also known as 3,4,5-Trimethylphenyl acetate, is an organic compound with the chemical formula C11H14O2. It is a colorless to pale yellow liquid with a strong, sweet, floral odor. This ester is formed by the reaction of 3,4,5-trimethylphenol with acetic acid, and it is commonly used as a fragrance ingredient in various applications, including perfumes, cosmetics, and household products. It is also employed as a flavoring agent in food and beverages, imparting a fruity, floral, and spicy taste. Due to its low toxicity and pleasant aroma, 3,4,5-trimethylphenyl acetate is a popular choice in the chemical industry for creating natural and synthetic scents.

6719-74-0

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6719-74-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6719-74-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,1 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6719-74:
(6*6)+(5*7)+(4*1)+(3*9)+(2*7)+(1*4)=120
120 % 10 = 0
So 6719-74-0 is a valid CAS Registry Number.

6719-74-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-acetoxy-1,2,3-trimethylbenzene

1.2 Other means of identification

Product number -
Other names 5-Acetoxy-hemellitol

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:6719-74-0 SDS

6719-74-0Relevant academic research and scientific papers

Substituent Effects on Intramolecular Selectivity and Free Energy Relationships in Anodic and Metal Ion Oxidations of 5-X-1,2,3-trimethylbenzenes

Baciocchi, Enrico,Cort, Antonella Dalla,Eberson, Lennart,Mandolini, Luigi,Rol, Cesare

, p. 4544 - 4548 (2007/10/02)

Side-chain oxidations, promoted electrochemically or chemically, by cerium(IV) ammonium nitrate (CAN) or cobalt(III) acetate, of 5-substituted-1,2,3-trimethylbenzenes have been investigated, and the relative reactivity of the 2- and 1-methyl group (k

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