Cas 791855-86-2,Oxiranecarboxamide, 3-methyl-N-[1-methyl-2-(1-piperidinyl)ethyl]-, (2S,3R)- (9CI)

791855-86-2

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Basic information

Product Name: Oxiranecarboxamide, 3-methyl-N-[1-methyl-2-(1-piperidinyl)ethyl]-, (2S,3R)- (9CI)
Synonyms: Oxiranecarboxamide, 3-methyl-N-[1-methyl-2-(1-piperidinyl)ethyl]-, (2S,3R)- (9CI)
CAS NO:791855-86-2
Molecular Formula: C₁₂H₂₂N₂O₂
Molecular Weight: 226.31528
EINECS: N/A
Product Categories: METHYL
Mol File: 791855-86-2.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 402.9±45.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 1.071±0.06 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 14.59±0.40(Predicted)
CAS DataBase Reference: Oxiranecarboxamide, 3-methyl-N-[1-methyl-2-(1-piperidinyl)ethyl]-, (2S,3R)- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Oxiranecarboxamide, 3-methyl-N-[1-methyl-2-(1-piperidinyl)ethyl]-, (2S,3R)- (9CI)(791855-86-2)
EPA Substance Registry System: Oxiranecarboxamide, 3-methyl-N-[1-methyl-2-(1-piperidinyl)ethyl]-, (2S,3R)- (9CI)(791855-86-2)

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: 791855-86-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 791855-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,8,5 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 791855-86:
(8*7)+(7*9)+(6*1)+(5*8)+(4*5)+(3*5)+(2*8)+(1*6)=222
222 % 10 = 2
So 791855-86-2 is a valid CAS Registry Number.

791855-86-2Upstream product

791855-86-2Downstream Products

791855-86-2Relevant academic research and scientific papers

Efficient solution phase parallel synthesis of norstatine analogs

Voronkov, Michael V.,Gontcharov, Alexander V.,Wang, Zhi-Min,Richardson, Paul F.,Kolb, Hartmuth C.

, p. 9043 - 9048 (2007/10/03)

The reaction of glycidic amides with various functionalized nitriles to afford norstatine analogs in a regio- and diastereoselective fashion (43-99% yield) is described. Utilizing this chemistry, a 20 membered solution phase library was prepared in two st

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