56401-31-1

Basic information

• Product Name: 1,10-Decanediol, mono(4-methylbenzenesulfonate)
• CAS NO: 56401-31-1
• Molecular Formula: C17H28O4S
• Molecular Weight: 328.473
• Mol File: 56401-31-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1,10-Decanediol, mono(4-methylbenzenesulfonate)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,10-Decanediol, mono(4-methylbenzenesulfonate)(56401-31-1)
• EPA Substance Registry System: 1,10-Decanediol, mono(4-methylbenzenesulfonate)(56401-31-1)

Safety Data

• Hazardous Substances Data: 56401-31-1(Hazardous Substances Data)

Upstream product

• 112-47-0 1,10-Decanediol 
• 98-59-9 p-toluenesulfonyl chloride 
• 83932-93-8 10-eicosenyl-1,20-ditosylate 

Downstream Products

• 57929-05-2 4-(10-Hydroxy-decyloxy)-benzonitrile 
• 119546-30-4 C₂₁H₃₂O₅S 
• 1233346-12-7 C₂₁H₃₀O₅ 
• 53179-04-7 undec-10-enenitrile 
• 188584-11-4 undec-10-ynyl-1-amine 
• 220568-93-4 4-((10-hydroxydecyl)oxy)benzaldehyde 
• 1201798-16-4 C₇H₇O₃S^(1-)*C₂₄H₅₂NO⁽¹⁺⁾ 
• 111040-37-0 10-hydroxydecyltrimethylammonium tosylate 
• 111040-51-8 2-benzyloxy-3-octadecyloxypropyl 10-trimethylammoniodecyl phosphate 

Relevant articles and documents

NUCLEOSIDE AND NUCLEOTIDE CONJUGATE COMPOUNDS AND USES THEREOF

This disclosure provides nucleoside and nucleotide conjugate compounds, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds in the treatment of conditions, diseases,

GALNAC DERIVATIVES

Modified oligonucleotides comprising a GalNAc moiety of the present disclosure along with methods of making and use, e.g., against HBV are disclosed.

Synthesis and biological activity of dialkylphosphocholines

A series of dialkylphosphocholines were prepared and evaluated for their biological activity. The antiprotozoal activity was determined against Acanthamoeba lugdunensis. Compound 15 exhibited excellent trophocidal activity. None of the tested dialkylphosphocholines exhibited better fungicidal activity against Candida albicans than miltefosine. The antineoplastic activity was determined against HeLa. The most cytotoxic was compound 10, which was more active against tumor cells as against normal cells.