1174540-21-6

Basic information

• Product Name: (R)-2-(N-1-(3-(4-chlorophenyl)pyrido[2,3-d]pyrimidin-4(3H)-one)-N-(1,1-dioxohexahydro-1λ6-thiopyran-4-yl)methyl)-2-(3-fluoro-4-(trifluoromethyl)phenyl)acetamide
• Synonyms: (R)-2-(N-1-(3-(4-chlorophenyl)pyrido[2,3-d]pyrimidin-4(3H)-one)-N-(1,1-dioxohexahydro-1λ6-thiopyran-4-yl)methyl)-2-(3-fluoro-4-(trifluoromethyl)phenyl)acetamide
• CAS NO: 1174540-21-6
• Molecular Weight: 651.081
• Mol File: 1174540-21-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (R)-2-(N-1-(3-(4-chlorophenyl)pyrido[2,3-d]pyrimidin-4(3H)-one)-N-(1,1-dioxohexahydro-1λ6-thiopyran-4-yl)methyl)-2-(3-fluoro-4-(trifluoromethyl)phenyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-(N-1-(3-(4-chlorophenyl)pyrido[2,3-d]pyrimidin-4(3H)-one)-N-(1,1-dioxohexahydro-1λ6-thiopyran-4-yl)methyl)-2-(3-fluoro-4-(trifluoromethyl)phenyl)acetamide(1174540-21-6)
• EPA Substance Registry System: (R)-2-(N-1-(3-(4-chlorophenyl)pyrido[2,3-d]pyrimidin-4(3H)-one)-N-(1,1-dioxohexahydro-1λ6-thiopyran-4-yl)methyl)-2-(3-fluoro-4-(trifluoromethyl)phenyl)acetamide(1174540-21-6)

Safety Data

• Hazardous Substances Data: 1174540-21-6(Hazardous Substances Data)

Upstream product

• 1174540-24-9 2-(1-chloroethyl)-3-(4-chlorophenyl)pyrido[2,3-d]pyrimidin-4(3H)-one 
• 1174540-23-8 3-(4-chlorophenyl)-2-ethylpyrido[2,3-d]pyrimidin-4(3H)-one 
• 1174540-26-1 2-(1-aminoethyl)-3-(4-chlorophenyl)pyrido[2,3-d]pyrimidin-4(3H)-one 
• 1174540-25-0 C₁₅H₁₁ClN₆O 
• 494210-61-6 1,1-dioxo-hexahydro-1λ⁶-thiopyran-4-carbaldehyde 
• 238754-67-1 2-(3-fluoro-4-(trifluoromethyl)phenyl)acetic acid 
• 1174540-28-3 2-((R)-(1-(1,1-dioxohexahydro-1λ6-thiopyran-4-yl)methylamino)ethyl)-3-(4-chlorophenyl)pyrido[2,3d]pyrimidin-4(3H)-one 
• 5345-47-1 2-aminopyridin-3-carboxylic acid 

Downstream Products

• 1262797-01-2 C₃₀H₂₇ClF₄N₄O₄S 

Relevant articles and documents

Practical syntheses of a CXCR3 antagonist

Two new, reliable syntheses of a pyrido[2,3-d]- pyrimidine inhibitor of the CXCR3 receptor are described. A nine-step synthesis of the CXCR3 inhibitor (1) from 2-aminonicotinic acid was demonstrated on a multikilogram scale and incorporates a classic reso