Cas 952117-50-9,(R,Z)-benzyl (1-(benzyloxycarbonyl)-2,3,6,7-tetrahydro-1H-azepin-3-yl)carbamate

952117-50-9

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Basic information

Product Name: (R,Z)-benzyl (1-(benzyloxycarbonyl)-2,3,6,7-tetrahydro-1H-azepin-3-yl)carbamate
Synonyms: (R,Z)-benzyl (1-(benzyloxycarbonyl)-2,3,6,7-tetrahydro-1H-azepin-3-yl)carbamate
CAS NO:952117-50-9
Molecular Formula:
Molecular Weight: 380.444
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: (R,Z)-benzyl (1-(benzyloxycarbonyl)-2,3,6,7-tetrahydro-1H-azepin-3-yl)carbamate(CAS DataBase Reference)
NIST Chemistry Reference: (R,Z)-benzyl (1-(benzyloxycarbonyl)-2,3,6,7-tetrahydro-1H-azepin-3-yl)carbamate(952117-50-9)
EPA Substance Registry System: (R,Z)-benzyl (1-(benzyloxycarbonyl)-2,3,6,7-tetrahydro-1H-azepin-3-yl)carbamate(952117-50-9)

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: 952117-50-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 952117-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,2,1,1 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 952117-50:
(8*9)+(7*5)+(6*2)+(5*1)+(4*1)+(3*7)+(2*5)+(1*0)=159
159 % 10 = 9
So 952117-50-9 is a valid CAS Registry Number.

952117-50-9Upstream product

952117-44-1 C₂₄H₂₈N₂O₄

952117-50-9Downstream Products

952117-58-7 C₂₇H₃₂N₂O₆

952117-50-9Relevant academic research and scientific papers

Dynamic kinetic asymmetric allylic amination and acyl migration of vinyl aziridines with imido carboxylates

Trost, Barry M.,Fandrick, Daniel R.,Brodmann, Tobias,Stiles, Dylan T.

, p. 6123 - 6125 (2008/09/16)

(Chemical Equation Presented) An atom-economical method has been developed for the preparation of chiral vicinal diamines through a dynamic kinetic asymmetric allylic amination and acyl-group migration of vinyl aziridines with imido carboxylates. Application of the asymmetric transformation enabled the concise synthesis of the azepane core 1 of (+)-balanol and its syn analogue.

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