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19666-03-6

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19666-03-6 Usage

General Description

Benzoic acid, 2-(1-oxobutyl)-, also known as 2-oxo-1-butoxybenzoic acid, is a chemical compound with the formula C11H12O3. It is a derivative of benzoic acid and is commonly used as a food preservative and flavoring agent. Benzoic acid, 2-(1-oxobutyl)- is also used in the production of pharmaceuticals, dyes, and plasticizers. It is a white crystalline solid that is soluble in organic solvents and has a slightly sweet odor. Benzoic acid, 2-(1-oxobutyl)- is regulated as a food additive and is generally recognized as safe for human consumption when used in accordance with good manufacturing practices.

Check Digit Verification of cas no

The CAS Registry Mumber 19666-03-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,6,6 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19666-03:
(7*1)+(6*9)+(5*6)+(4*6)+(3*6)+(2*0)+(1*3)=136
136 % 10 = 6
So 19666-03-6 is a valid CAS Registry Number.

19666-03-6SDS

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 2-butanoylbenzoic acid

1.2 Other means of identification

Product number -
Other names 2-butanoyl-benzoic acid

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:19666-03-6 SDS

19666-03-6Relevant articles and documents

-

Ullyot et al.

, p. 429,434 (1945)

-

Enantioselective Palladium(II)-Catalyzed Intramolecular Aminoarylation of Alkenes by Dual N?H and Aryl C?H Bond Cleavage

Zhang, Wen,Chen, Pinhong,Liu, Guosheng

supporting information, p. 5336 - 5340 (2017/04/27)

An asymmetric palladium-catalyzed intramolecular oxidative aminoarylation of alkenes has been developed with quinoline–oxazoline chiral ligands and Ag2CO3 as the oxidant. Various indolines containing a quaternary stereogenic center were synthesized in high yield with excellent enantioselectivity. Preliminary mechanistic studies suggest that the addition of a catalytic amount of phenylglyoxylic acid significantly accelerates the reaction and slightly enhances the enantioselectivity.

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