125968-55-0

Basic information

• Product Name: 2-amino-4,6-bis(p-methoxyphenyl)pyrimidine
• Synonyms: 2-amino-4,6-bis(p-methoxyphenyl)pyrimidine
• CAS NO: 125968-55-0
• Molecular Weight: 307.352
• Mol File: 125968-55-0.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-amino-4,6-bis(p-methoxyphenyl)pyrimidine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-4,6-bis(p-methoxyphenyl)pyrimidine(125968-55-0)
• EPA Substance Registry System: 2-amino-4,6-bis(p-methoxyphenyl)pyrimidine(125968-55-0)

Safety Data

• Hazardous Substances Data: 125968-55-0(Hazardous Substances Data)

Upstream product

• 105782-42-1 (2RS,3SR)-2,3-epoxy-1-(4-methoxyphenyl)-3-(4-methoxyphenyl)propan-1-one 
• 124-46-9 guanidine hydrogen carbonate 
• 2373-89-9 4,4'-dimethoxychalcone 
• 41564-67-4 (E)-1,3-bis(4-methoxyphenyl)-2-propene-1-one 
• 123-11-5 4-methoxy-benzaldehyde 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 50-01-1 guanidine hydrochloride 
• 3319-15-1 rac-1-(4-methoxyphenyl)-ethanol 
• 113-00-8 guanidine nitrate 
• 105-13-5 4-Methoxybenzyl alcohol 
• 56-05-3 2-Amino-4,6-dichloropyrimidine 
• 5720-07-0 4-methoxyphenylboronic acid 
• 1000385-94-3 C₁₁H₁₀N₃ClSO₃ 

Downstream Products

• 24030-15-7 4,6-bis(4-methoxyphenyl)pyrimidin-2-ol 
• 1226781-10-7 C₃₃H₃₆N₄O₁₁S 
• 125968-57-2 5-amino-4,6-bis(p-methoxyphenyl)pyrimidine 
• 125968-56-1 5-nitroso-4,6-bis(p-methoxyphenyl)pyrimidine 

Relevant articles and documents

A green approach for the synthesis of benzazolyl pyrimidinyl carbamothioates under ultrasonication and their antimicrobial activity

A library of benzazolyl pyrimidinyl carbamothioates were prepared by the reaction of benzazolyl carbonothioates with pyrimidinyl-2-amine in the presence of an ionic liquid- 1-butyl-3-methylimidazolium hydroxide ([bmim]OH) under ultrasonication at a frequency of 35?kHz and tested for antimicrobial activity. Chloro- and nitro-substituted benzothiazolyl/benzimidazolyl pyrimidinyl carbamothioates displayed prominent antibacterial activity against Bacillus subtilis, while nitro-substituted benzothiazolyl/benzimidazolyl pyrimidinyl carbamothioates showed excellent antifungal activity against Aspergilus niger. Graphic abstract: [Figure not available: see fulltext.].

Mechanistic investigations on substituted benzene sulphonamides as apoptosis inducing anticancer agents

In an approach to develop potent cytotoxic compounds with targeted action, a systematic methodology was employed to design and initially synthesize parent compounds A1, A8, A13 and A14 followed by synthesis of further analogs of A1 (A2-A7) and A8 (A9-A12)

Influence of the C-5 substitution in polysubstituted pyrimidines on inhibition of prostaglandin E2 production

As a part of a broader structure-activity relationship study of substituted 2-aminopyrimidines, the influence of the C-5 substitution on inhibition of prostaglandin E2 (PGE2) production was studied. Thirty compounds were prepared sta