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2-Quinazolinecarboxylic acid, 1,2,3,4-tetrahydro-2-methyl-4-oxo-, is a chemical compound belonging to the quinazolinecarboxylic acid class. It is a derivative of quinazoline, featuring a tetrahydrofuran ring with a methyl and oxo group attached to it. This unique structure and its properties make it a promising candidate for research and development in the pharmaceutical industry, particularly for the creation of new drugs.

129768-69-0

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129768-69-0 Usage

Uses

Used in Pharmaceutical Industry:
2-Quinazolinecarboxylic acid, 1,2,3,4-tetrahydro-2-methyl-4-oxo-, is used as a key intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its unique structure allows for the development of drugs with novel mechanisms of action and potential therapeutic benefits.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2-Quinazolinecarboxylic acid, 1,2,3,4-tetrahydro-2-methyl-4-oxo-, serves as a valuable compound for further exploration and development. Researchers utilize its properties to design and synthesize new drug candidates with improved pharmacological profiles, targeting a wide range of diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 129768-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,7,6 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 129768-69:
(8*1)+(7*2)+(6*9)+(5*7)+(4*6)+(3*8)+(2*6)+(1*9)=180
180 % 10 = 0
So 129768-69-0 is a valid CAS Registry Number.

129768-69-0SDS

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 2-methyl-4-oxo-1,3-dihydroquinazoline-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Quinazolinecarboxylic acid,1,2,3,4-tetrahydro-2-methyl-4-oxo

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:129768-69-0 SDS

129768-69-0Downstream Products

129768-69-0Relevant academic research and scientific papers

Synthesis of chrysogine, a metabolite of Penicillium chrysogenum and some related 2-substituted 4-(3H)-quinazolinones

Bergman, Jan,Brynolf, Anna

, p. 1295 - 1310 (2007/10/02)

Syntheses of both enantiomers of chrysogine, 2-(α-hydroxyethyl)-4(3H)-quinazolinone, 1 from 2-ammobenzamide are reported. Thus reaction of 2-aminobenzamide and optically active α-acetoxypropionyl chloride gave 9, which upon saponification and cyclization induced by aqueous sodium carbonate at room temperature gave chrysogine. The enantiomeric purity of 1 was determined by NMR. Inversion of (-)-(S)-1, using the Mitsunobo reaction, gave (+)-(R)-1. Reduction of 2-acetyl-4(3H)-qumazolinone 2 with baker's yeast gave the S-enantiomer of 1. The cyclization method used could be extended and a number of 2-(a-hydroxy)alkyl-4-(3H)-quinazolinones are also reported.

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