59549-51-8

Basic information

• Product Name: 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE
• Synonyms: 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE;5-Bromo-2-chloro-4-(methylsulphanyl)pyrimidine;5-Bromo-2-chloro-4-(methylsulfanyl)pyrimidine;5-Bromo-2-chloro-4-(methylsulphanyl)pyrimidine, 5-Bromo-2-chloro-4-(methylthio)-1,3-diazine;5-Bromo-2-chloro-4-(methylthio)
• CAS NO: 59549-51-8
• Molecular Formula: C₅H₄BrClN₂S
• Molecular Weight: 239.52
• Product Categories: Building Blocks;Pyrimidine
• Mol File: 59549-51-8.mol
• Article Data: 6

Chemical Properties

• Melting Point: 56-58℃
• Boiling Point: 346.1 °C at 760 mmHg
• Flash Point: 163.1 °C
• Appearance: /
• Density: 1.83
• Vapor Pressure: 0.000118mmHg at 25°C
• Refractive Index: 1.649
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: -1.87±0.29(Predicted)
• CAS DataBase Reference: 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE(59549-51-8)
• EPA Substance Registry System: 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE(59549-51-8)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 59549-51-8(Hazardous Substances Data)

Usage

General Description

5-Bromo-2-chloro-4-(methylthio)pyrimidine is a chemical compound with the molecular formula C5H4BrClN2S. It is a heterocyclic compound containing a pyrimidine ring with bromine, chlorine, and a methylthio group attached to it. 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE has potential applications in the field of pharmaceuticals and agrochemicals, where it can be used as a building block for the synthesis of various biologically active compounds. It is also used as a reagent in organic synthesis to introduce the 2-chloro-4-(methylthio)pyrimidine group into other molecules. 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE is known for its moderate toxicity and should be handled with care in a laboratory setting.

InChI:InChI=1/C5H4BrClN2S/c1-10-4-3(6)2-8-5(7)9-4/h2H,1H3

Upstream product

• 36082-50-5 2,4-dichloro-5-bromopyrimidine 
• 5188-07-8 sodium thiomethoxide 

Downstream Products

• 917896-40-3 2-methyl-4-methylsulfanyl-5-(4-trifluoromethyl-phenyl)-pyrimidine 
• 1403865-31-5 5-bromo-N-(1-methylcyclopropyl)-4-(methylthio)pyrimidin-2-amine 
• 1220417-45-7 (5-bromo-4-methylsulfanyl-pyrimidin-2-yl)-(3-chloro-4-fluorophenyl)-amine 
• 1034358-66-1 N-(5-bromo-4-methylsulphanylpyrimidin-2-yl)-N'-pyrimidin-2-yl-benzene-1,4-diamine 

Relevant articles and documents

JNK inhibitor as well as pharmaceutical composition and application thereof

The invention provides a compound represented by a formula (I), racemates, stereoisomers, tautomers, isotope markers, solvates, polymorphic substances, nitrogen oxides, or pharmaceutically acceptablesalts thereof, and application as a JNK inhibitor. The invention also provides a preparation method of the compound shown in the formula (I), a pharmaceutical composition containing the compound shownin the formula (I), and application of the compound shown in the formula (I) to preparation of a medicine, and the medicine is used for treating diseases which can be treated by inhibiting the activity of JNK.

NOVEL HETARYL-PHENYLENEDIAMINE-PYRIMIDINES AS PROTEIN KINASE INHIBITORS

The invention relates to novel hetaryl-phenylenediamine-pyrimidines and to their structurally related oxygen and sulphur analogues of the general formula I, processes for their preparation, and their use as medicaments.

Sulfoximine-substituted pyrimidines, processes for production thereof and use thereof as drugs

The invention relates to sulfoximine-substituted pyrimidines of the general formula I processes for the preparation thereof and their use as drugs.