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5-Iodo-6-methyl-2-(methylthio)-1H-pyrimidin-4-one is a chemical compound with the molecular formula C6H7IN2OS. It is a derivative of pyrimidin-4-one, featuring a methyl group at the 6th position, an iodine atom at the 5th position, and a methylthio group at the 2nd position. 5-Iodo-6-methyl-2-(methylthio)-1H-pyrimidin-4-one is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the development of new drugs. Its unique structure allows for further functionalization and modification, making it a valuable intermediate in organic synthesis.

76510-64-0

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76510-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76510-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,1 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76510-64:
(7*7)+(6*6)+(5*5)+(4*1)+(3*0)+(2*6)+(1*4)=130
130 % 10 = 0
So 76510-64-0 is a valid CAS Registry Number.

76510-64-0SDS

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 5-iodo-6-methyl-2-methylsulfanyl-1H-pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 5-Iodo-6-methyl-2-methylsulfanyl-pyrimidin-4-ol

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:76510-64-0 SDS

76510-64-0Relevant academic research and scientific papers

Substituted pyridine and pyrimidine derivatives and their use in treating viral infections

-

, (2016/09/26)

The present invention provides compounds of Formula (I): and tautomers, isomers, and esters of said compounds, and pharmaceutically acceptable salts, solvates, and prodrugs of said compounds, wherein each of R, R1, X, Y, Z, R2, R3, R4, R5, R6, R7, R8, R9, R18, R19 and n is selected independently and as defined herein. Compositions comprising such compounds are also provided. The compounds of the invention are effective as inhibitors of HCV, and are useful, alone and together with other therapeutic agents, in treating or preventing diseases or disorders such as viral infections and virus-related disorders.

Synthesis and SAR of pyridothiazole substituted pyrimidine derived HCV replication inhibitors

Girijavallabhan, Vinay M.,Alvarez, Carmen,Bennett, Frank,Chen, Lei,Gavalas, Stephen,Huang, Yuhua,Kim, Seong-Heon,Kosinski, Aneta,Pinto, Patrick,Rizvi, Razia,Rossman, Randall,Shankar, Bandarpalle,Tong, Ling,Velazquez, Francisco,Venkatraman, Srikanth,Verma, Vishal A.,Kozlowski, Joseph,Shih, Neng-Yang,Piwinski, John J.,MacCoss, Malcolm,Kwong, Cecil D.,Bansal, Namita,Clark, Jeremy L.,Fowler, Anita T.,Kezar III, Hollis S.,Valiyaveettil, Jacob,Reynolds, Robert C.,Maddry, Joseph A.,Ananthan, Subramaniam,Secrist III, John A.,Li, Cheng,Chase, Robert,Curry, Stephanie,Huang, Hsueh-Cheng,Tong, Xiao,Njoroge, F. George,Arasappan, Ashok

, p. 5652 - 5657 (2012/09/22)

Introduction of a nitrogen atom into the benzene ring of a previously identified HCV replication (replicase) benzothiazole inhibitor 1, resulted in the discovery of the more potent pyridothiazole analogues 3. The potency and PK properties of the compounds were attenuated by the introductions of various functionalities at the R1, R2 or R3 positions of the molecule (compound 3). Inhibitors 38 and 44 displayed excellent potency, selectivity (GAPDH/MTS CC50), PK parameters in all species studied, and cross genotype activity.

SUBSTITUTED PYRIDINE AND PYRIMIDINE DERIVATIVES AND THEIR USE IN TREATING VIRAL INFECTIONS

-

, (2010/04/03)

The present invention provides compounds of Formula (I): and tautomers, isomers, and esters of said compounds, and pharmaceutically acceptable salts, solvates, and prodrugs of said compounds, wherein wherein each of R, R1, X, Y, Z, R2, R3, R4, R5, R6, R7, R8, R9, R18, R19 and n is selected independently and as defined herein. Compositions comprising such compounds are also provided. The compounds of the invention are effective as inhibitors of HCV, and are useful, alone and together with other therapeutic agents, in treating or preventing diseases or disorders such as viral infections and virus-related disorders.

CONDENSED HETEROAROMATIC RING SYSTEMS. VII. SYNTHESIS OF THIENOPYRIDINES, THIENOPYRIMIDINES, AND FUROPYRIDINES FROM o-SUBSTITUTED N-HETEROARYLACETYLENES

Sakamoto, Takao,Kondo, Yoshinori,Watanabe, Ryo,Yamanaka, Hiroshi

, p. 2719 - 2724 (2007/10/02)

The cross-coupling reaction of 2-chloro-3-iodo- and 4-chloro-3iodopyridines with phenylacetylene in the presence of dichlorobis(triphenylphosphine)palladium occured at the 3-position.The 3-ethynylpyridines containing an adjacent chloro group were converti

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