Cas 928776-81-2,tert-butyl (1S,2S)-N-[2-(N'-benzyl-N'-methylamino)cyclopentyl]carbamate

928776-81-2

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Basic information

Product Name: tert-butyl (1S,2S)-N-[2-(N'-benzyl-N'-methylamino)cyclopentyl]carbamate
Synonyms: tert-butyl (1S,2S)-N-[2-(N'-benzyl-N'-methylamino)cyclopentyl]carbamate
CAS NO:928776-81-2
Molecular Formula:
Molecular Weight: 304.433
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: tert-butyl (1S,2S)-N-[2-(N'-benzyl-N'-methylamino)cyclopentyl]carbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (1S,2S)-N-[2-(N'-benzyl-N'-methylamino)cyclopentyl]carbamate(928776-81-2)
EPA Substance Registry System: tert-butyl (1S,2S)-N-[2-(N'-benzyl-N'-methylamino)cyclopentyl]carbamate(928776-81-2)

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: 928776-81-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 928776-81-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,8,7,7 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 928776-81:
(8*9)+(7*2)+(6*8)+(5*7)+(4*7)+(3*6)+(2*8)+(1*1)=232
232 % 10 = 2
So 928776-81-2 is a valid CAS Registry Number.

928776-81-2Upstream product

928776-81-2Downstream Products

928776-91-4 (1S,2S)-N-benzyl-N-methylcyclopentane-1,2-diamine

928776-81-2Relevant academic research and scientific papers

A biocatalytic approach to synthesizing optically active orthogonally protected trans-cyclopentane-1,2-diamine derivatives

Gonzalez-Sabin, Javier,Gotor, Vicente,Rebolledo, Francisca

, p. 1309 - 1314 (2007)

(Chemical Equation Presented) A straightforward chemoenzymatic synthesis of optically active trans-N,N-dialkylcyclopentane-1,2-diamines has been efficiently developed starting out from their analogous (±)-trans-2-(N,N- dialkylamino)-cyclopentanols. The ro

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