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66162-60-5

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66162-60-5 Usage

General Description

ETHYL 3,4,5-TRIMETHOXYPHENYL ACETATE is a chemical compound that belongs to the class of aromatic esters. It is commonly used in the fragrance industry as a synthetic aroma compound, providing a sweet and floral scent. This chemical is also used in the production of perfumes, soaps, and other scented products. It is important to handle this chemical with care, as it can be irritating to the skin and eyes, and may cause respiratory issues if inhaled in high concentrations. While it is generally considered safe for use in small quantities, proper safety measures should be taken when working with ETHYL 3,4,5-TRIMETHOXYPHENYL ACETATE.

Check Digit Verification of cas no

The CAS Registry Mumber 66162-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,1,6 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66162-60:
(7*6)+(6*6)+(5*1)+(4*6)+(3*2)+(2*6)+(1*0)=125
125 % 10 = 5
So 66162-60-5 is a valid CAS Registry Number.

66162-60-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(3,4,5-trimethoxyphenyl)acetate

1.2 Other means of identification

Product number -
Other names OR3002

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:66162-60-5 SDS

66162-60-5Relevant articles and documents

Substituted benzylidene tetrahydronaphthalene derivative and its preparation method, application

-

Paragraph 0069; 0070, (2017/08/02)

The invention relates to substituted benzylidene tetralone derivatives and a preparation method and application. The chemical structural formula of the substituted benzylidene tetralone derivatives is shown in the formula (1) in the specification, and in

Unusual Tethering Effects in the Schmidt Reaction of Hydroxyalkyl Azides with Ketones: Cation-π and Steric Stabilization of a Pseudoaxial Phenyl Group

Katz, Christopher E.,Aube, Jeffrey

, p. 13948 - 13949 (2007/10/03)

The Lewis acid-promoted reactions of chiral 2-aryl-3-azido-1-propanols with 4-substituted cyclohexanones lead to iminium ethers and ultimately caprolactams (following a hydrolysis step). In this study, it is shown that these reactions afford variable ratios of products, depending on the electronic nature of the phenyl group. These results are interpreted in the context of a cation?π stabilizing effect in the product-determining reaction intermediate. Remarkably, the best selectivity was obtained when an azidopropanol reagent containing a quaternary center was used; a control experiment showed that the high selectivity observed in this result depended upon the free rotation of the pseudoaxial aromatic group in the intermediate that affords the major product. Copyright

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