Cas 1440109-77-2,(3R,4R)-3-acetoxy-1-(benzyloxycarbonyl)-4-(tert-butoxycarbonylamino)pyrrolidine

1440109-77-2

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Basic information

Product Name: (3R,4R)-3-acetoxy-1-(benzyloxycarbonyl)-4-(tert-butoxycarbonylamino)pyrrolidine
Synonyms: (3R,4R)-3-acetoxy-1-(benzyloxycarbonyl)-4-(tert-butoxycarbonylamino)pyrrolidine
CAS NO:1440109-77-2
Molecular Formula:
Molecular Weight: 378.425
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: (3R,4R)-3-acetoxy-1-(benzyloxycarbonyl)-4-(tert-butoxycarbonylamino)pyrrolidine(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4R)-3-acetoxy-1-(benzyloxycarbonyl)-4-(tert-butoxycarbonylamino)pyrrolidine(1440109-77-2)
EPA Substance Registry System: (3R,4R)-3-acetoxy-1-(benzyloxycarbonyl)-4-(tert-butoxycarbonylamino)pyrrolidine(1440109-77-2)

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: 1440109-77-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1440109-77-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,0,1,0 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1440109-77:
(9*1)+(8*4)+(7*4)+(6*0)+(5*1)+(4*0)+(3*9)+(2*7)+(1*7)=122
122 % 10 = 2
So 1440109-77-2 is a valid CAS Registry Number.

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1440109-77-2Relevant academic research and scientific papers

Chemoenzymatic synthesis of orthogonally protected (3R,4R)- and (3S,4S)-trans-3-amino-4-hydroxypyrrolidines

Rodríguez-Rodríguez, Jesús A.,Quijada, F. Javier,Brieva, Rosario,Rebolledo, Francisca,Gotor, Vicente

, p. 5407 - 5412 (2013/07/05)

Several orthogonally protected racemic trans-3-amino-4-hydroxypyrrolidines have been easily prepared from N-Cbz-3,4-epoxypyrrolidine. Resolution of each racemic compound was accomplished by means of lipase-catalyzed aminolysis, transesterification or hydr

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