Cas 856258-22-5,(1S,5S,1'S,2'S)-1-acetoxy-5-[2,3-bis(benzyloxy)-1-tert-butoxycarbonylaminopropyl]cyclopent-2-ene

856258-22-5

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Basic information

Product Name: (1S,5S,1'S,2'S)-1-acetoxy-5-[2,3-bis(benzyloxy)-1-tert-butoxycarbonylaminopropyl]cyclopent-2-ene
Synonyms: (1S,5S,1'S,2'S)-1-acetoxy-5-[2,3-bis(benzyloxy)-1-tert-butoxycarbonylaminopropyl]cyclopent-2-ene
CAS NO:856258-22-5
Molecular Formula:
Molecular Weight: 495.616
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (1S,5S,1'S,2'S)-1-acetoxy-5-[2,3-bis(benzyloxy)-1-tert-butoxycarbonylaminopropyl]cyclopent-2-ene(CAS DataBase Reference)
NIST Chemistry Reference: (1S,5S,1'S,2'S)-1-acetoxy-5-[2,3-bis(benzyloxy)-1-tert-butoxycarbonylaminopropyl]cyclopent-2-ene(856258-22-5)
EPA Substance Registry System: (1S,5S,1'S,2'S)-1-acetoxy-5-[2,3-bis(benzyloxy)-1-tert-butoxycarbonylaminopropyl]cyclopent-2-ene(856258-22-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 856258-22-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 856258-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,2,5 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 856258-22:
(8*8)+(7*5)+(6*6)+(5*2)+(4*5)+(3*8)+(2*2)+(1*2)=195
195 % 10 = 5
So 856258-22-5 is a valid CAS Registry Number.

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856258-22-5Relevant academic research and scientific papers

Synthesis of L-Carbafuranomycin, an unnatural analogue of the antibiotic amino acid furanomycin

Ja, Young Lee,Schiffer, Guido,Jaeger, Volker

, p. 2317 - 2320 (2007/10/03)

(Chemical Equation Presented) L-(+)-Carbafuranomycin is a novel analogue of L-(+)-furanomycin, an unusual antibiotic α-amino acid that attracted great interest due to its activity as an isoleucine antagonist. We present here a concise and efficient asymme

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