Cas 289716-59-2,(S)-2-{[(1R,4R)-4-Acetoxycyclopent-2-enyl](toluene-4-sulfonyl)amino}pent-4-enoic acid methyl ester

289716-59-2

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Basic information

Product Name: (S)-2-{[(1R,4R)-4-Acetoxycyclopent-2-enyl](toluene-4-sulfonyl)amino}pent-4-enoic acid methyl ester
Synonyms: (S)-2-{[(1R,4R)-4-Acetoxycyclopent-2-enyl](toluene-4-sulfonyl)amino}pent-4-enoic acid methyl ester
CAS NO:289716-59-2
Molecular Formula:
Molecular Weight: 407.488
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: (S)-2-{[(1R,4R)-4-Acetoxycyclopent-2-enyl](toluene-4-sulfonyl)amino}pent-4-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-{[(1R,4R)-4-Acetoxycyclopent-2-enyl](toluene-4-sulfonyl)amino}pent-4-enoic acid methyl ester(289716-59-2)
EPA Substance Registry System: (S)-2-{[(1R,4R)-4-Acetoxycyclopent-2-enyl](toluene-4-sulfonyl)amino}pent-4-enoic acid methyl ester(289716-59-2)

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: 289716-59-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 289716-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,9,7,1 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 289716-59:
(8*2)+(7*8)+(6*9)+(5*7)+(4*1)+(3*6)+(2*5)+(1*9)=202
202 % 10 = 2
So 289716-59-2 is a valid CAS Registry Number.

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289716-59-2Relevant academic research and scientific papers

Enantioselective synthesis of α,α'-disubstituted piperidines via ruthenium-catalyzed ring rearrangement

Voigtmann, Ulrike,Blechert, Siegfried

, p. 893 - 898 (2007/10/03)

A new method for the enantioselective synthesis of α,α'-disubstituted piperidines is described. Easily available cyclopentenones 5a,b rearrange via Ru-catalyzed RCM-ROM to heterocycles. Compound 6a is converted to the indolizidine 13.

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