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4-nitro-N-(2-oxo-2,3-dihydropyrimidin-4-yl)benzamide is a complex organic compound with the molecular formula C12H10N4O4. It is a derivative of benzamide, featuring a nitro group at the 4-position and a 2-oxo-2,3-dihydropyrimidin-4-yl group attached to the nitrogen atom. 4-nitro-N-(2-oxo-2,3-dihydropyrimidin-4-yl)benzamide is characterized by its yellow crystalline appearance and is soluble in organic solvents such as dimethyl sulfoxide (DMSO). It has been studied for its potential applications in medicinal chemistry, particularly as an inhibitor of certain enzymes or as a building block in the synthesis of more complex molecules. The compound's structure and properties make it a subject of interest for researchers exploring new therapeutic agents and chemical reactions.

7472-61-9

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7472-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7472-61-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7472-61:
(6*7)+(5*4)+(4*7)+(3*2)+(2*6)+(1*1)=109
109 % 10 = 9
So 7472-61-9 is a valid CAS Registry Number.

7472-61-9SDS

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 4-nitro-N-(2-oxo-1H-pyrimidin-6-yl)benzamide

1.2 Other means of identification

Product number -
Other names 4-Nitro-benzoesaeure-(2-oxo-1,2-dihydro-pyrimidin-4-ylamid)

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:7472-61-9 SDS

7472-61-9Relevant academic research and scientific papers

Stereoselective N-glycosylation with N4-acyl cytosines and efficient synthesis of gemcitabine

Liu, Tongchao,Tang, Jiadeng,Liang, Jianpeng,Chen, Yabin,Wang, Xiaowen,Shen, Jingkang,Zhao, Dongmei,Xiong, Bing,Cen, Jun-Da,Chen, Yue-Lei

, p. 1203 - 1213 (2019/01/29)

Through systematical comparison of various N4-protected cytosine derivatives in the glycosylation step of gemcitabine synthesis, highly beta-stereoselective and high yielding TBAI catalyzed N-glycosylation was achieved with N4-Bz cytosine and anomeric mixture of 2,2‘-difluororibose mesylate donor. The subsequent global deprotection gave gemcitabine efficiently. Meanwhile, the anomeric chloride intermediate and fluoride-displaced side products of this N-glycosylation were identified, too. This new glycosylation method reveals the importance of N4-protection in the stereoselective preparation of pyrimidine nucleoside, also provides a potential alternative to current industrial process to gemcitabine.

Preparation method of cytidine

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Paragraph 0057-0060, (2019/12/10)

The invention provides a preparation method of cytidine 1, which comprises the following steps: (1) carrying out a condensation reaction on a compound 6 and a compound 7 in the presence of stannic chloride to generate a compound 8; (2) removing an alpha-isomer and other reaction impurities in the compound 8 to obtain the beta-isomer compound 8; and (3) carrying out a deprotection reaction on the beta-isomer compound 8 in the presence of an alcohol solvent, and then carrying out a salt forming reaction with hydrochloric acid to obtain a compound 1. The nucleoside compound 8 can be obtained withhigh beta-stereoselectivity starting from a cheap raw material 7 with a mixed anomeric carbon configuration, especially the raw material 7a, and a slightly excessive basic group 6, especially the basic group 6a; the trace alpha-compound 8 isomer impurities can be removed from the nucleoside compound 8 through a simple pulping method; and subsequently, deprotection and salifying reactions for beta-compound 8 have high yield, so that the method can reduce the production cost of the compound 1.

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