Cas 282527-07-5,(S)-6-Benzyloxy-1-(toluene-4-sulfonyl)-1,2,3,6-tetrahydro-pyridine-2-carboxylic acid methyl ester

282527-07-5

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Basic information

Product Name: (S)-6-Benzyloxy-1-(toluene-4-sulfonyl)-1,2,3,6-tetrahydro-pyridine-2-carboxylic acid methyl ester
Synonyms: (S)-6-Benzyloxy-1-(toluene-4-sulfonyl)-1,2,3,6-tetrahydro-pyridine-2-carboxylic acid methyl ester
CAS NO:282527-07-5
Molecular Formula:
Molecular Weight: 401.483
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)-6-Benzyloxy-1-(toluene-4-sulfonyl)-1,2,3,6-tetrahydro-pyridine-2-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-6-Benzyloxy-1-(toluene-4-sulfonyl)-1,2,3,6-tetrahydro-pyridine-2-carboxylic acid methyl ester(282527-07-5)
EPA Substance Registry System: (S)-6-Benzyloxy-1-(toluene-4-sulfonyl)-1,2,3,6-tetrahydro-pyridine-2-carboxylic acid methyl ester(282527-07-5)

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: 282527-07-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 282527-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,2,5,2 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 282527-07:
(8*2)+(7*8)+(6*2)+(5*5)+(4*2)+(3*7)+(2*0)+(1*7)=145
145 % 10 = 5
So 282527-07-5 is a valid CAS Registry Number.

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282527-07-5Relevant academic research and scientific papers

A ring-closing metathesis-mediated route to novel enantiopure conformationally restricted cyclic amino acids

Tjen, Kim C. M. F.,Kinderman, Sape S.,Schoemaker, Hans E.,Hiemstra, Henk,Rutjes, Floris P. J. T.

, p. 699 - 700 (2007/10/03)

A combination of palladium-catalysed N,O-acetal formation, ruthenium- catalysed ring-closing metathesis and N-sulfonyliminium ion-mediated C-C bond formation constitutes an efficient and versatile route to a set of enantiomerically pure 2,6-disubstituted unsaturated pipecolic acid derivatives.

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