114634-29-6

Basic information

• Product Name: Toluene-4-sulfonic acid (S)-3-hydroxy-hexadecyl ester
• Synonyms: Toluene-4-sulfonic acid (S)-3-hydroxy-hexadecyl ester
• CAS NO: 114634-29-6
• Molecular Weight: 412.634
• Mol File: 114634-29-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Toluene-4-sulfonic acid (S)-3-hydroxy-hexadecyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Toluene-4-sulfonic acid (S)-3-hydroxy-hexadecyl ester(114634-29-6)
• EPA Substance Registry System: Toluene-4-sulfonic acid (S)-3-hydroxy-hexadecyl ester(114634-29-6)

Safety Data

• Hazardous Substances Data: 114634-29-6(Hazardous Substances Data)

Upstream product

• 114634-28-5 (+)-(S)-hexadecane-1,3-diol 
• 98-59-9 p-toluenesulfonyl chloride 
• 112-64-1 tetradecanoyl chloride 
• 114634-27-4 (S)-3-Hydroxy-hexadecanoic acid (1S,2R,3R,4S)-4,7,7-trimethyl-3-naphthalen-1-yl-bicyclo[2.2.1]hept-2-yl ester 
• 114634-26-3 4,7,7-trimethyl-3-exo-(1-naphthyl)bicyclo<2.2.1>hept-2-exo-yl 3-oxohexadecanoate 
• 14427-53-3 methyl 3-oxohexadecanoate 

Downstream Products

• 32778-77-1 solenopsin B 

Relevant articles and documents

Enantioselective Construction of Heterocycles: Synthesis of (R,R)-Solenopsin B

An enantioselective route to solenopsin B (1) , the major saturated component of the alkaloid mixture isolated from the venom of the fire ant, Solenopsis invicta, is reported.The key transformation in this synthesis is the smooth thermolytic cyclization of alkenyl azide 3.The precursor to 3, alcohol 4, is prepared by stereoselective reduction of an enantiomerically pure β-keto ester.