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5449-42-3

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5449-42-3 Usage

General Description

Ethyl 2-hydroxy-3,3-diphenylpropanoate is a chemical compound with the molecular formula C21H22O3. It is an ester that consists of a hydroxy group and a carboxylic acid functional group. ethyl 2-hydroxy-3,3-diphenylpropanoate is commonly used as a flavoring agent in the food industry, imparting a sweet and fruity taste. It is also used in the production of perfumes and cosmetics due to its pleasant aroma. Additionally, ethyl 2-hydroxy-3,3-diphenylpropanoate has potential applications in pharmaceuticals and as a raw material in chemical synthesis. However, it should be handled with care as it may cause irritation to the skin and eyes upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 5449-42-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5449-42:
(6*5)+(5*4)+(4*4)+(3*9)+(2*4)+(1*2)=103
103 % 10 = 3
So 5449-42-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H18O3/c1-2-20-17(19)16(18)15(13-9-5-3-6-10-13)14-11-7-4-8-12-14/h3-12,15-16,18H,2H2,1H3

5449-42-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-hydroxy-3,3-diphenylpropanoate

1.2 Other means of identification

Product number -
Other names 2-hydroxy-3,3-diphenyl-propionic acid ethyl ester

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:5449-42-3 SDS

5449-42-3Relevant articles and documents

Metal-free ring-opening of epoxides with potassium trifluoroborates

Roscales, Silvia,Csaky, Aurelio G.

supporting information, p. 454 - 456 (2014/01/06)

The ring-opening of epoxides with potassium trifluoroborates proceeds smoothly in the presence of trifluoroacetic anhydride under metal-free conditions. The reactions are regioselective and afford a single diastereomer. Both electron-rich and electron-poor aryltrifluoroborates are tolerated.

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