128595-07-3

Basic information

• Product Name: N-(Cyclopentyloxycarbonyloxy)succinimide
• Synonyms: CYCLOPENTYL SUCCINIMIDYL CARBONATE;CPOC-OSU;1-[[(CYCLOPENTYLOXY)CARBONYL]OXY]-2,5-PYRROLIDINEDIONE;2,5-PYRROLIDINEDIONE,1-[[(CYCLOPENTYLOXY)CARBONYL]OXY]-;N-(CYCLOPENTYLOXY CARBONYLOXY) SUCCINIMIDE;N-(CYCLOPENTYLOXYCARBONYL)SUCCINIMIDE;Cyclipentylsuccinimidyl Carbonate;N-(CYCLOPENTYLOXY CURBONYLOXY) SUCCINIMIDE
• CAS NO: 128595-07-3
• Molecular Formula: C₁₀H₁₃NO₅
• Molecular Weight: 227.21
• EINECS: 1533716-785-6
• Product Categories: Pharmaceutical Intermediates;Amino Acid Derivatives
• Mol File: 128595-07-3.mol
• Article Data: 2

Chemical Properties

• Melting Point: 78.0 to 82.0 °C
• Boiling Point: 320 °C at 760 mmHg
• Flash Point: 147.4 °C
• Appearance: /
• Density: 1.35 g/cm³
• Vapor Pressure: 0.000326mmHg at 25°C
• Refractive Index: 1.532
• Storage Temp.: 0-10°C
• CAS DataBase Reference: N-(Cyclopentyloxycarbonyloxy)succinimide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(Cyclopentyloxycarbonyloxy)succinimide(128595-07-3)
• EPA Substance Registry System: N-(Cyclopentyloxycarbonyloxy)succinimide(128595-07-3)

Safety Data

• Statements: 36/37/38
• Hazardous Substances Data: 128595-07-3(Hazardous Substances Data)

Usage

Chemical Properties

White to almost white crystalline powder

InChI:InChI=1/C10H13NO5/c12-8-5-6-9(13)11(8)16-10(14)15-7-3-1-2-4-7/h7H,1-6H2

Upstream product

• 74124-79-1 di(succinimido) carbonate 
• 96-41-3 Cyclopentanol 

Downstream Products

• 145631-04-5 [(1S,2S,4R)-1-Benzyl-2-hydroxy-4-((1S,2R)-2-hydroxy-indan-1-ylcarbamoyl)-5-phenyl-pentyl]-carbamic acid cyclopentyl ester 
• 1001096-38-3 C₃₈H₄₅BrF₂N₃O₁₁PS 
• 572924-00-6 N-[(cyclopentyloxy)carbonyl]-L-tert-leucine 
• 1426688-43-8 cyclopentyl-3-((3-(4-(methylsulfonamido)phenyl)-4-oxo-4H-chromen-7-yl)ethynyl)azetidine-1-carboxylate 

Relevant articles and documents

Highly efficient carbamate formation from alcohols and hindered amino acids or esters using N, N′-disuccinimidyl carbonate (DSC)

A highly efficient and straightforward protocol to prepare carbamates from alcohols and hindered amino acids/esters mediated by N,N′-disuccinimidyl carbonate (DSC) in the presence of catalytic amount of pyridine is described. This method could be carried out under mild conditions in one pot, and a wide variety of carbamates were obtained in high yield with excellent purity. Georg Thieme Verlag Stuttgart - New York.