199486-81-2

Basic information

• Product Name: N-1-(p-toluenesulfonyl)cytosine
• Synonyms: N-1-(p-toluenesulfonyl)cytosine
• CAS NO: 199486-81-2
• Molecular Weight: 265.293
• Mol File: 199486-81-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-1-(p-toluenesulfonyl)cytosine(CAS DataBase Reference)
• NIST Chemistry Reference: N-1-(p-toluenesulfonyl)cytosine(199486-81-2)
• EPA Substance Registry System: N-1-(p-toluenesulfonyl)cytosine(199486-81-2)

Safety Data

• Hazardous Substances Data: 199486-81-2(Hazardous Substances Data)

Upstream product

• 2240-25-7 5-bromocytosine 
• 98-59-9 p-toluenesulfonyl chloride 
• 1122-44-7 5-iodocytosine 
• 79628-80-1 4-(1,1,1,3,3,3-Hexamethyl-disilazan-2-yl)-2-trimethylsilanyloxy-pyrimidine 
• 71-30-7 Cytosine 

Downstream Products

• 1159258-17-9 Pd(1-(p-toluenesulfonyl)cytosine-N₃)2Cl₂ 
• 919524-54-2 5-(morpholin-4-ylmethyl)cytosine 
• 6339-26-0 4-tosylmorpholine 
• 1159258-18-0 Pd₂(1-(p-toluenesulfonyl)cytosine-N₃,N₄^(1-))4 
• 1159258-19-1 Pd₂(1-(p-toluenesulfonyl)cytosine-N₃,N₄^(1-))2Cl₂(DMSO)2 
• 1193656-89-1 dichlorobis[1-(p-toluenesulfonyl)cytosine]cobalt(II) 
• 1193656-88-0 dichlorobis[1-(p-toluenesulfonyl)cytosine]cadmium(II) 
• 1193656-86-8 dichlorobis[1-(p-toluenesulfonyl)cytosine]copper(II) 

Relevant articles and documents

Synthesis of the sulfonylpyrimidine derivatives as a new type of sulfonylcycloureas

The synthesis of several novel N-1 and N-1,NH-4-disulfonylpyrimidine derivatives are described.

Antiproliferative and proapoptotic activity of molecular copper(II) complex of N-1-tosylcytosine

In an attempt to enhance the previously observed antiproliferative capacity of 1-(p-toluenesulfonyl)cytosine (N-1-tosylcytosine, ligand 1), its copper(II) complex (Cu(1-TsC-N3)2Cl2, complex 2) was prepared and tested in vitro on vari

5-bromo- and 5-iodo-N-1-sulfonylated cytosine derivatives. Exclusive formation of keto-imino tautomers

N-1-Sulfonylated cytosine 5 and 5-halogeno-N-1-sulfonylated cytosine derivatives 1 and 2 were synthesized by condensation of silylated cytosine or 5-halogenocytosine bases with tosylchloride in acetonitrile, or by the reaction of cytosine or 5-halogenocyt