78596-73-3

Basic information

• Product Name: phloroglucinol dibenzyl ether monobenzenesulfonate
• Synonyms: phloroglucinol dibenzyl ether monobenzenesulfonate
• CAS NO: 78596-73-3
• Molecular Weight: 446.524
• Mol File: 78596-73-3.mol

Chemical Properties

• CAS DataBase Reference: phloroglucinol dibenzyl ether monobenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: phloroglucinol dibenzyl ether monobenzenesulfonate(78596-73-3)
• EPA Substance Registry System: phloroglucinol dibenzyl ether monobenzenesulfonate(78596-73-3)

Safety Data

• Hazardous Substances Data: 78596-73-3(Hazardous Substances Data)

Upstream product

• 3840-04-8 1,3,5-tris<(benzenesulfonyl)oxy>benzene 
• 100-44-7 benzyl chloride 
• 3900-81-0 phloroglucinol monobenzenesulfonate 

Downstream Products

• 78596-82-4 3-((p-bromobenzenesulfonyl)oxy)-3a-acetoxy-4-(benzyloxy)-6-methoxy-2,3,3a,8a-tetrahydrofuro<2,3-b>benzofuran 
• 78596-81-3 3-((p-bromobenzenesulfonyl)oxy)-3a-hydroxy-4-(benzyloxy)-6-methoxy-2,3,3a,8a-tetrahydrofuro<2,3-b>benzofuran 
• 78596-76-6 3-acetoxy-3a-bromo-4,6-bis(benzyloxy)-2,3,3a,8a-tetrahydrofuro<2,3-b>benzofuran 
• 78596-77-7 3,3a-acetonide-4,6-bis(benzyloxy)-2,3,3a,8a-tetrahydrofuro<2,3-b>benzofuran 
• 78596-85-7 3,3a-dihydroxy-4,6-bis(benzyloxy)-2,3,3a,8a-tetrahydrofuro<2,3-b>benzofuran 
• 78596-79-9 3,3a-acetonide-4-(benzyloxy)-6-methoxy-2,3,3a,8a-tetrahydrofuro<2,3-b>benzofuran 
• 78596-78-8 3,3a-acetonide-4-(benzyloxy)-6-hydroxy-2,3,3a,8a-tetrahydrofuro<2,3-b>benzofuran 
• 78596-80-2 3,3a-dihydroxy-4-(benzyloxy)-6-methoxy-2,3,3a,8a-tetrahydrofuro<2,3-b>benzofuran 
• 63604-98-8 1,3-dibenzylphloroglucinol 

Relevant articles and documents

Organosilyl-Benzo-triazole derivatives, processes for their production and their use as UV protecting agents

The present invention refers to new benzotriazole derivatives, which for their physicochemical properties can be used as UV protection agents. In addition, they can be used to manufacture cosmetic, dermatological, veterinarian as well as pharmaceutical formulations, which protect the skin, lips, nails and hair against UV radiation.

A New Synthesis of Aflatoxin M1

Starting with the known and readily available phloroglucinol monobenzenesulfonate (4) and 1,4-anhydroerythritol (7), we prepared aflatoxin M1 (1) in 13 steps with an overall yield of 5percent.The critical features of this second synthesis of aflatoxin M1 (1) include a novel approach to the tricyclic phenol 21 containing the ABC ring system, a regioselective hydrogenolysis of the benzyl protecting group at C6 in 16, and removal of the second benzyl group in 20 by Birch reduction.Neither the 1,3,5-trialkoxy-substituted benzene ring nor the vinyl ether function present in 20 were affected in the latter operation.