16325-43-2

Basic information

• Product Name: 3,4-Dihydro-4,4,6-trimethyl-1-phenyl-2(1H)-pyrimidinethione
• Synonyms: 3,4-Dihydro-4,4,6-trimethyl-1-phenyl-2(1H)-pyrimidinethione;USAF K-1796;1,4-DIHYDRO-1-PHENYL-4,4,6-TRIMETHYL-2-PYRIMIDINETHIOL
• CAS NO: 16325-43-2
• Molecular Formula: C₁₃H₁₆N₂S
• Molecular Weight: 232.3445
• Mol File: 16325-43-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 314.9°Cat760mmHg
• Flash Point: 144.3°C
• Appearance: /
• Density: 1.16g/cm³
• Vapor Pressure: 0.000452mmHg at 25°C
• Refractive Index: 1.635
• CAS DataBase Reference: 3,4-Dihydro-4,4,6-trimethyl-1-phenyl-2(1H)-pyrimidinethione(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-Dihydro-4,4,6-trimethyl-1-phenyl-2(1H)-pyrimidinethione(16325-43-2)
• EPA Substance Registry System: 3,4-Dihydro-4,4,6-trimethyl-1-phenyl-2(1H)-pyrimidinethione(16325-43-2)

Safety Data

• Hazardous Substances Data: 16325-43-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H16N2S/c1-10-9-13(2,3)14-12(16)15(10)11-7-5-4-6-8-11/h4-9H,1-3H3,(H,14,16)

Upstream product

• 62-53-3 aniline 
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• 141-79-7 4-methyl-pent-3-en-2-one 
• 1147550-11-5 ammonium thiocyanate 
• 66647-68-5 4-bromo-4-methylpentan-2-one 

Downstream Products

• 69939-65-7 7,7-dichloro-2-phenyl-1,5,5-trimethyl-2,4-diazabicyclo<4.1.0>heptane-3-thione 
• 74628-49-2 6-hydroxy-4,4,6-trimethyl-1-phenyltetrahydropyrimidine-2(1H)-thione 
• 34927-74-7 1,4-dihydro-4,4,6-trimethyl-2-methylthio-1-phenylpyrimidine 
• 27058-61-3 2-phenylamino-4,4,6-trimethyl-4H-1,3-thiazine 
• 85961-00-8 1,4-dihydro-4,4,6-trimethyl-1-phenylpyrimidine 
• 58913-46-5 6,6-dimethyl-4-(phenylamino)-5,6-dihydropyridine-2(1H)-thione 
• 103-85-5 monophenylthiourea 
• 34928-12-6 4,4,6-trimethyl-1-phenyl-1,4-dihydropyrimidine-2(3H)-one 
• 5392-23-4 3,4-dihydro-4,4,6-trimethylpyrimidine-2(1H)-thione 
• 74732-54-0 3,5-Diphenyl-3H-thiazol-2-one 
• 1010-53-3 3-phenyl-2,4-thiazolidinedione 
• 85311-52-0 2-benzylsulfanyl-4,4,6-trimethyl-1-phenyl-1,4-dihydro-pyrimidine 
• 78725-17-4 1-phenyl-3-ethoxycarbonyl-4,4,6-trimethyl-1,4-dihydropyrimidine-2(3H)thione 
• 69939-64-6 7,7-dichloro-3-<(dichloromethyl)thio>-2-phenyl-1,5,5-trimethyl-2,4-diazabicyclo<4.1.0>hept-3-ene 

Relevant articles and documents

Synthesis of Polynitroaryl Derivatives of 3-Aryl-1H,4H-dihydro-4,6,6-trimethyl-pyrimidine-2-thiols as Possible Fungicides

Fortyeight new 3-aryl-1,4-dihydro-2-polynitroarylmercapto-4,6,6-trimethylpyrimidines (1-6) have been prepared in good yields by the condensation of appropriate active chlorobenzene and pyrimidine-2-thiol (A) in the presence of anhydrous sodium acetate in

Organometallic Compounds. XI. Chlorotrimethylsilane / Sodium Bromide - A Simple System for the in situ Generation of Bromotrimethylsilane. Reaction with Ketones, Sulfoxides, and Various Oxygen Containing Substrates

Bromotrimethylsilane is generated in situ by the addition of chlorotrimethylsilane (2) to a solution or a suspension of sodium bromide (or LiBr, KBr, MgBr2).The reaction of the in situ generated bromotrimethylsilane with ketones, sulfoxides, γ-butyrolactone, triethyl orthoformate, and trialkyl phosphites is described.