Cas 1417826-95-9,(S)-1-(3-benzylmorpholino)-3-(2-nitrophenyl)propan-1-one

1417826-95-9

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Basic information

Product Name: (S)-1-(3-benzylmorpholino)-3-(2-nitrophenyl)propan-1-one
Synonyms: (S)-1-(3-benzylmorpholino)-3-(2-nitrophenyl)propan-1-one
CAS NO:1417826-95-9
Molecular Formula:
Molecular Weight: 354.406
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: (S)-1-(3-benzylmorpholino)-3-(2-nitrophenyl)propan-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-(3-benzylmorpholino)-3-(2-nitrophenyl)propan-1-one(1417826-95-9)
EPA Substance Registry System: (S)-1-(3-benzylmorpholino)-3-(2-nitrophenyl)propan-1-one(1417826-95-9)

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: 1417826-95-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1417826-95-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,7,8,2 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1417826-95:
(9*1)+(8*4)+(7*1)+(6*7)+(5*8)+(4*2)+(3*6)+(2*9)+(1*5)=179
179 % 10 = 9
So 1417826-95-9 is a valid CAS Registry Number.

1417826-95-9Upstream product

7684-27-7 3-benzylmorpholine

1417826-95-9Downstream Products

1417826-95-9Relevant academic research and scientific papers

KINETIC RESOLUTION OF CHIRAL AMINES

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Page/Page column 111; 112; 113, (2013/03/26)

The present invention refers to a method for the kinetic resolution of a chiral primary or secondary amine by treating the amine with a chiral, hydroxamic acid derived reagent of the formula (I). These chiral reagents are particularly useful for the kinetic resolution of cyclic amines and may be generated in situ in the presence of an N-heterocyclic carbene, thus allowing for a catalytic reaction.

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