Cas 1000072-81-0,(R)-2-(((2R,3S)-3-((tert-butyldimethylsilyloxy)methyl)aziridin-2-yl)methylamino)-3-methyl-N-phenylbutanamide

1000072-81-0

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Basic information

Product Name: (R)-2-(((2R,3S)-3-((tert-butyldimethylsilyloxy)methyl)aziridin-2-yl)methylamino)-3-methyl-N-phenylbutanamide
Synonyms: (R)-2-(((2R,3S)-3-((tert-butyldimethylsilyloxy)methyl)aziridin-2-yl)methylamino)-3-methyl-N-phenylbutanamide
CAS NO:1000072-81-0
Molecular Formula:
Molecular Weight: 391.629
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)-2-(((2R,3S)-3-((tert-butyldimethylsilyloxy)methyl)aziridin-2-yl)methylamino)-3-methyl-N-phenylbutanamide(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-(((2R,3S)-3-((tert-butyldimethylsilyloxy)methyl)aziridin-2-yl)methylamino)-3-methyl-N-phenylbutanamide(1000072-81-0)
EPA Substance Registry System: (R)-2-(((2R,3S)-3-((tert-butyldimethylsilyloxy)methyl)aziridin-2-yl)methylamino)-3-methyl-N-phenylbutanamide(1000072-81-0)

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: 1000072-81-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1000072-81-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,0,7 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1000072-81:
(9*1)+(8*0)+(7*0)+(6*0)+(5*0)+(4*7)+(3*2)+(2*8)+(1*1)=60
60 % 10 = 0
So 1000072-81-0 is a valid CAS Registry Number.

1000072-81-0Upstream product

160334-53-2 (R)-N'-phenyl 2-amino-3-methylbutanamide

1000072-81-0Downstream Products

1000072-81-0Relevant academic research and scientific papers

Epimerization- and protecting-group-free synthesis of peptidomimetic conjugates from amphoteric amino aldehydes

Li, Xinghan,Yudin, Andrei K.

, p. 14152 - 14153 (2008/09/16)

We have developed a novel protecting-group-free strategy for the synthesis of peptidomimetic conjugates. The high degrees of stereocontrol and chemoselectivity achieved in this chemistry hinge upon unusual preferences of the amphoteric amino aldehydes. Th

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