33109-58-9

Basic information

• Product Name: Butanedioic acid, bis(4-nitrophenyl) ester
• CAS NO: 33109-58-9
• Molecular Formula: C16H12N2O8
• Molecular Weight: 360.28
• Mol File: 33109-58-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Butanedioic acid, bis(4-nitrophenyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: Butanedioic acid, bis(4-nitrophenyl) ester(33109-58-9)
• EPA Substance Registry System: Butanedioic acid, bis(4-nitrophenyl) ester(33109-58-9)

Safety Data

• Hazardous Substances Data: 33109-58-9(Hazardous Substances Data)

Upstream product

• 621-14-7 diphenyl succinate 
• 100-02-7 4-nitro-phenol 
• 543-20-4 succinoyl dichloride 
• 110-15-6 succinic acid 
• 108-30-5 succinic acid anhydride 
• 5070-13-3 bis-(p-nitrophenyl) carbonate 

Downstream Products

• 132610-14-1 (+)-(2S)-2-<4-<3-(p-nitrophenoxycarbonyl)propionamido>butyl>-1,4,7-triazacyclononane-1,4,7-triyltris 
• 141380-96-3 1-<3-<3-(p-nitrophenoxycarbonyl)propionamido>propylphosphinicomethyl>-1,4,7,10-tetraazacyclododecane-4,7,10-triyltris 
• 141380-89-4 (+)-(2S)-2-<4-<3-(p-nitrophenoxycarbonyl)propionamido>butyl>-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetrayltetrakis 
• 71-27-2 succinylcholine chloride 
• 1609647-56-4 succinic acid bis(4-isocyanatophenyl) ester 
• 1609647-55-3 succinic acid bis(4-aminophenyl) ester 

Relevant articles and documents

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A novel L-lysine based multifunctional crosslinker family was developed and utilized to fabricate a 100% pure poly(ester amide) (PEA) hydrogel with unique structure via a novel gelation strategy in a single and rapid step. Enzyme triggered biodegradation

PROCESS FOR PREPARATION OF SUCCINYLCHOLINE CHLORIDE

The invention discloses a novel process for preparation of succinylcholine chloride via transesterification of succinic acid diester with choline chloride.

BIODEGRADABLE WATER SOLUBLE POLYMERS

The invention provides biodegradable, water soluble PEA, PEUR and PEU carrier polymers, which can be used to conjugate, and thereby stabilize and/or solublize, bioactive agents via polar uncharged or charged groups and activated ester or amino groups cont