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5-Pyrimidinecarbonitrile, 1,4-dihydro-2-(methylthio)-4-oxo-6-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97693-21-5

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97693-21-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97693-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,6,9 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 97693-21:
(7*9)+(6*7)+(5*6)+(4*9)+(3*3)+(2*2)+(1*1)=185
185 % 10 = 5
So 97693-21-5 is a valid CAS Registry Number.

97693-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylsulfanyl-4-oxo-6-phenyl-1H-pyrimidine-5-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-hydroxy-2-(methylsulfanyl)-6-phenyl-5-pyrimidinecarbonitrile

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:97693-21-5 SDS

97693-21-5Relevant academic research and scientific papers

Design, synthesis, and antihypertensive activity of new pyrimidine derivatives endowing new pharmacophores

Farghaly, Ahmed M.,AboulWafa, Omaima M.,Elshaier, Yaseen A. M.,Badawi, Waleed A.,Haridy, Haridy H.,Mubarak, Heba A. E.

, p. 360 - 379 (2019/02/03)

A new series of achiral pyrimidine derivatives based on nifedipine-like structure was designed and synthesized. These pyrimidyl derivatives contained hydrazine, hydrazones, acetohydrazide, differently substituted benzylidene functionalities, benzosulfohyd

Synthesis and Anti-HBV Activity of Novel Substituted Pyrimidine Glycosides and Their Acyclic Analogues

Hawata,El-Sayed,Abdel-Rahman, Adel A.-H.

, p. 1734 - 1744 (2018/11/10)

New aryl substituted uracil and thiouracil glycosides are synthesized by glycosylation at N1 in the pyrimidine nucleus using glycopyranosyl halides in basic medium. In addition C-linked hydrazinyl acyclic sugar derivatives exhibiting different

Vasoactive thiomethyl-pyrimidines: Promising drug candidates with vascular activity

De Andrade, Audrey N.,Araújo, Alice V.,Barbosa, Hugo B.W.,Wanderley, Almir G.,Malta, Oscar L.,Dos Anjos, Janaína V.

, p. 1266 - 1273 (2017/06/06)

Pyrimidines and their derivatives are present in various biologically active molecules. Most of the synthetic methods employed to achieve the pyrimidinone ring consist of two stages: The synthesis of a Michael intermediate from an aldehyde and an "active

Synthesis, antiplasmodial activity and mechanistic studies of pyrimidine-5-carbonitrile and quinoline hybrids

Kaur, Hardeep,Balzarini, Jan,De Kock, Carmen,Smith, Peter J.,Chibale, Kelly,Singh, Kamaljit

, p. 52 - 62 (2015/06/30)

Abstract A series of hybrids comprising of 5-cyanopyrimidine and quinoline moiety were synthesized and tested for in vitro antiplasmodial activity against NF54 and Dd2 strains of Plasmodium falciparum. Hybrid bearing m-nitrophenyl substituent at C-4 of py

Synthesis and antiviral activity of new substituted pyrimidine glycosides

Ramiz, Mahmoud M. M.,El-Sayed, Wael A.,Hagag, Ezzat,Abdel-Rahman, Adel A.-H.

experimental part, p. 1028 - 1038 (2011/11/29)

A number of N-substituted pyrimidine glycosides were synthesized by coupling reaction of the pyrimidine base with acetobromosugars followed by deprotection. The synthesized compounds were tested for their antiviral activity against Hepatitis B Virus (HBV). Plaque reduction infectivity assay was used to determine virus count reduction as a result of treatment with tested compounds which showed moderate to high anti viral activities.

Glycosylation of 2-thiouracil derivatives. A synthetic approach to 3- glycosyl-2,4-dioxypyrimidines

Khodair,Ibrahim,El Ashry

, p. 433 - 444 (2007/10/03)

Reaction of 6-aryl-5-cyano-2-thiouracils 2a-d with glycosyl halides 4a,b under alkaline conditions gave the respective bisglycosylated derivatives 5a- h. However, their deacetylation with ammonia in methanol caused a cleavage of the S-glycosyl residue and gave the N-3 glycosylated analogues 6a-h.

A One-Step Synthesis of 2-Methylthio-6-oxopyrimidine Derivatives: Preparation of Fused Pyrimidinones

Hussain, S. M.,El-Barbary, A. A.,Mansour, S. A.

, p. 169 - 171 (2007/10/02)

Condensation of a ternary mixture of ethyl cyanoacetate, S-methylisothiourea and aromatic aldehydes in pyridine afforded directly the 4-aryl-5-cyano-6-oxopyrimidines IV in good yields.Alkylation of IV with alkyl halides in alkaline medium yielded the 1-al

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