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125867-32-5

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125867-32-5 Usage

Description

2-Pivaloylamino-3-benzoylpyridine, with the CAS number 125867-32-5, is a white solid compound that is primarily utilized in the field of organic synthesis. Its unique chemical structure allows it to serve as a valuable building block or intermediate in the creation of more complex organic molecules.

Uses

Used in Organic Synthesis:
2-Pivaloylamino-3-benzoylpyridine is used as a synthetic building block for the development of various organic compounds. Its application in this field is due to its versatile chemical properties, which enable it to be a part of multiple chemical reactions and contribute to the formation of a wide range of molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Pivaloylamino-3-benzoylpyridine is used as a key intermediate in the synthesis of potential drug candidates. Its unique structure and reactivity make it a valuable component in the development of new medications, particularly those targeting specific biological pathways or receptors.
Used in Chemical Research:
2-Pivaloylamino-3-benzoylpyridine is also employed in chemical research as a model compound to study various reaction mechanisms and to understand the behavior of similar molecules under different conditions. This helps researchers to gain insights into the properties and potential applications of related compounds.
Used in Material Science:
In the field of material science, 2-Pivaloylamino-3-benzoylpyridine can be used as a component in the development of novel materials with specific properties, such as improved stability, reactivity, or selectivity. Its incorporation into these materials can lead to advancements in various applications, including catalysis, sensors, and energy storage devices.

Check Digit Verification of cas no

The CAS Registry Mumber 125867-32-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,8,6 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 125867-32:
(8*1)+(7*2)+(6*5)+(5*8)+(4*6)+(3*7)+(2*3)+(1*2)=145
145 % 10 = 5
So 125867-32-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H18N2O2/c1-17(2,3)16(21)19-15-13(10-7-11-18-15)14(20)12-8-5-4-6-9-12/h4-11H,1-3H3,(H,18,19,21)

125867-32-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Pivaloylamino-3-benzoylpyridine

1.2 Other means of identification

Product number -
Other names N-(3-benzoylpyridin-2-yl)-2,2-dimethylpropanamide

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:125867-32-5 SDS

125867-32-5Relevant articles and documents

Synthesis and structure-activity relationship studies on a novel series of naphthylidinoylureas as inhibitors of acyl-CoA:cholesterol O-acyltransferase (ACAT)

Ohnuma, Satoshi,Muraoka, Masami,Ioriya, Katsuhisa,Ohashi, Naohito

, p. 1309 - 1311 (2007/10/03)

The synthesis and structure-activity relationships of N-phenyl-N′-[3- (4-phenylnaphthylidinoyl)]urea derivatives 3 as a novel structural class of potent ACAT inhibitors is described. A 3-methoxy group substituted on the naphthylidinone 4-phenyl ring, toge

Synthesis of ortho-substituted aminopyridines. Metalation of pivaloylamino derivatives

Estel,Linard,Marsais,Godard,Queguiner

, p. 105 - 112 (2007/10/02)

The three isomeric pivaloylaminopyridines were lithiated in more than 80% yields. Aminopyridine derivatives were treated by 2.5-3 equivalents of the complex BuLi-TMEDA at -10° in diethyl ether. Reaction of the lithiated species with various electrophiles afforded a number of ortho-substituted pivaloylaminopyridines in good yields. Secondary pyridine alcohols were oxidized to the corresponding aminopyridyl ketones. Pyridopyrimidines, benzonaphthyridines as well as an analogue of the natural antitumor alkaloid ellipticine has been synthesized showing the versatility of the method.

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