Cas 1262870-49-4,(2S)-N-((+/-)-trans-1-benzyl-6-oxo-2-phenylpiperidin-3-yl)-3-phenyl-2-(2,2,2-trifluoroacetamido)propanamide

1262870-49-4

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Basic information

Product Name: (2S)-N-((+/-)-trans-1-benzyl-6-oxo-2-phenylpiperidin-3-yl)-3-phenyl-2-(2,2,2-trifluoroacetamido)propanamide
Synonyms:
CAS NO:1262870-49-4
Molecular Formula:
Molecular Weight: 523.555
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: (2S)-N-((+/-)-trans-1-benzyl-6-oxo-2-phenylpiperidin-3-yl)-3-phenyl-2-(2,2,2-trifluoroacetamido)propanamide(CAS DataBase Reference)
NIST Chemistry Reference: (2S)-N-((+/-)-trans-1-benzyl-6-oxo-2-phenylpiperidin-3-yl)-3-phenyl-2-(2,2,2-trifluoroacetamido)propanamide(1262870-49-4)
EPA Substance Registry System: (2S)-N-((+/-)-trans-1-benzyl-6-oxo-2-phenylpiperidin-3-yl)-3-phenyl-2-(2,2,2-trifluoroacetamido)propanamide(1262870-49-4)

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: 1262870-49-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1262870-49-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,8,7 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1262870-49:
(9*1)+(8*2)+(7*6)+(6*2)+(5*8)+(4*7)+(3*0)+(2*4)+(1*9)=164
164 % 10 = 4
So 1262870-49-4 is a valid CAS Registry Number.

1262870-49-4Upstream product

350-09-4 N-trifluoroacetyl-L-phenylalanine

1262870-49-4Downstream Products

1262870-49-4Relevant academic research and scientific papers

Synthesis of piperidinones incorporating an amino acid moiety as potential SP antagonists

Burdzhiev, Nikola,Stanoeva, Elena

experimental part, p. 1443 - 1449 (2011/10/05)

Substituted (±)-trans-1-benzyl-6-oxo-2-phenylpiperidine-3- carboxamides (type I) and the acylated derivatives of (±)-trans-5-amino- 1-benzyl-6-phenylpiperidin-2-one (type II) were prepared by the reaction of (±)-trans-1-benzyl-6-oxo-2-phenylpiperidine-3-c

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