83166-76-1

Basic information

• Product Name: 5-[(2,4-Diamino-5-pyrimidinyl)methyl]-2-methoxyphenol
• Synonyms: 2,4-Diamino-5-[3-hydroxy-4-methoxybenzyl]pyrimidine;5-[(2,4-Diamino-5-pyrimidinyl)methyl]-2-methoxyphenol
• CAS NO: 83166-76-1
• Molecular Formula: C₁₂H₁₄N₄O₂
• Molecular Weight: 0
• Mol File: 83166-76-1.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-[(2,4-Diamino-5-pyrimidinyl)methyl]-2-methoxyphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 5-[(2,4-Diamino-5-pyrimidinyl)methyl]-2-methoxyphenol(83166-76-1)
• EPA Substance Registry System: 5-[(2,4-Diamino-5-pyrimidinyl)methyl]-2-methoxyphenol(83166-76-1)

Safety Data

• Hazardous Substances Data: 83166-76-1(Hazardous Substances Data)

Upstream product

• 78233-99-5 2,4-diamino-5-(3-benzyloxy-4-methoxybenzyl)-pyrimidine 
• 7440-44-0 pyrographite 
• 7440-05-3 palladium 

Downstream Products

• 128076-26-6 5-(3-{3-[4-(4-Amino-benzenesulfonyl)-phenylamino]-propoxy}-4-methoxy-benzyl)-pyrimidine-2,4-diamine 
• 111452-90-5 5-(3-{2-[4-(4-Amino-benzenesulfonyl)-phenylamino]-ethoxy}-4-methoxy-benzyl)-pyrimidine-2,4-diamine 
• 111452-89-2 5-{3-[4-(4-Amino-benzenesulfonyl)-benzyloxy]-4-methoxy-benzyl}-pyrimidine-2,4-diamine 
• 111452-96-1 5-{4-Methoxy-3-[4-(4-nitro-benzenesulfonyl)-benzyloxy]-benzyl}-pyrimidine-2,4-diamine 
• 111452-86-9 5-(4-Methoxy-3-{3-[4-(4-nitro-benzenesulfonyl)-phenylamino]-propoxy}-benzyl)-pyrimidine-2,4-diamine 
• 111452-85-8 5-(4-Methoxy-3-{2-[4-(4-nitro-benzenesulfonyl)-phenylamino]-ethoxy}-benzyl)-pyrimidine-2,4-diamine 

Relevant articles and documents

Substituted 2,4-diamino-5-benzylpyrimidines, their preparation and their use as medicaments with an antimicrobial activity

Novel substituted 2,4-diamino-5-benzyl pyrimidines are described. The novel substances have antimicrobial activity and are particularly suitable for inhibiting the growth of mycobacteria. Combined with inhibitors such as diaminodiphenylsulphones, ring-substituted 4-aminodiphenylsulphones or ring and/or nitrogen-substituted diaminodiphenylsulphones, they have a marked synergistic activity.