26547-31-9

Basic information

• Product Name: 2-[(4-chlorophenyl)sulfanyl]pyrimidine
• Synonyms: Pyrimidine, 2-(p-chlorophenylthio)-; Pyrimidine, 2-(p-chlorophenylthio)-,
• CAS NO: 26547-31-9
• Molecular Formula: C₁₀H₇ClN₂S
• Molecular Weight: 222.694
• Mol File: 26547-31-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 395.3°C at 760 mmHg
• Flash Point: 192.9°C
• Density: 1.37g/cm³
• Vapor Pressure: 4.24E-06mmHg at 25°C
• Refractive Index: 1.664
• CAS DataBase Reference: 2-[(4-chlorophenyl)sulfanyl]pyrimidine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(4-chlorophenyl)sulfanyl]pyrimidine(26547-31-9)
• EPA Substance Registry System: 2-[(4-chlorophenyl)sulfanyl]pyrimidine(26547-31-9)

Safety Data

• Hazardous Substances Data: 26547-31-9(Hazardous Substances Data)

Upstream product

• 637-87-6 1-Chloro-4-iodobenzene 
• 131242-36-9 2-sulfanylpyrimidine 
• 106-46-7 para-dichlorobenzene 
• 89523-62-6 (4-chlorophenyl)zinc(II) chloride 
• 106-39-8 bromochlorobenzene 

Relevant articles and documents

Copper-Catalyzed Electrophilic Thiolation of Organozinc Halides by Using N-Thiophthalimides Leading to Polyfunctional Thioethers

(Hetero)aryl, benzylic, and alkyl zinc halides were thiolated with N-thiophthalimides at 25 °C within 1 h in the presence of 5–10 % Cu(OAc)2?H2O to furnish the corresponding polyfunctionalized thioethers in good yields. This electrop

Phenylthioheterocyclic derivatives

Compounds of the formula STR1 wherein n is a integer of 0 to 2; R1 ' and R2 ' are, independently, hydrogen, halogen, trifluoromethyl, lower alkoxy or lower alkyl; and X is pyrimidinyl, thiazolyl or STR2 wherein R is hydrogen, lower alkyl, aryl or ar-lower alkyl; provided that at least one or R1 ' and R2 ' is other than hydrogen, and their pharmaceutically acceptable acid addition salts, and an anti-inflammatory method utilizing a compound of the formula STR3 wherein n is an integer of 0 to 2; R1 and R2 are, independently, hydrogen, halogen, trifluoromethyl, nitro, amino, lower alkylamino, di-lower-alkylamino, lower alkoxy or lower alkyl; and X is pyrimidinyl, thiazolyl or STR4 wherein R is hydrogen, lower alkyl, aryl or ar-lower alkyl; and their pharmaceutically acceptable acid addition salts, are described.