Cas 140933-96-6,(4-Methoxy-benzyl)-((1S,4R,5S,6S)-4,5,6-tris-benzyloxy-cyclohex-2-enyl)-thiocarbamic acid S-benzyl ester

140933-96-6

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Basic information

Product Name: (4-Methoxy-benzyl)-((1S,4R,5S,6S)-4,5,6-tris-benzyloxy-cyclohex-2-enyl)-thiocarbamic acid S-benzyl ester
Synonyms:
CAS NO:140933-96-6
Molecular Formula:
Molecular Weight: 685.884
EINECS: N/A
Product Categories: N/A
Mol File: 140933-96-6.mol
Article Data: 1

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: (4-Methoxy-benzyl)-((1S,4R,5S,6S)-4,5,6-tris-benzyloxy-cyclohex-2-enyl)-thiocarbamic acid S-benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4-Methoxy-benzyl)-((1S,4R,5S,6S)-4,5,6-tris-benzyloxy-cyclohex-2-enyl)-thiocarbamic acid S-benzyl ester(140933-96-6)
EPA Substance Registry System: (4-Methoxy-benzyl)-((1S,4R,5S,6S)-4,5,6-tris-benzyloxy-cyclohex-2-enyl)-thiocarbamic acid S-benzyl ester(140933-96-6)

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: 140933-96-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 140933-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,9,3 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 140933-96:
(8*1)+(7*4)+(6*0)+(5*9)+(4*3)+(3*3)+(2*9)+(1*6)=126
126 % 10 = 6
So 140933-96-6 is a valid CAS Registry Number.

140933-96-6Upstream product

140933-95-5 C₄₃H₄₃NO₅S

140933-96-6Downstream Products

140933-96-6Relevant articles and documents

INTRAMOLECULAR AMINO DELIVERY REACTIONS FOR THE SYNTHESIS OF VALIENAMINE AND ANALOGUES

Knapp, Spencer,Naughton, Andrew B. J.,Dhar, T. G. Murali

, p. 1025 - 1028 (1992)

Iodocyclization and sigmatropic rearrangement reactions of N-substituted carbonimidothioates are used to prepare valienamine (1), 7-norvalienamine (8), and the valienamine-based pseudo-disaccharide 12. Key words: carbonimidothioates; iodocyclization; rearrangement; glucosidase inhibitors; pseudo disaccharides

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