Cas 881422-63-5,2-Oxazolidinone, 3-[(3S)-3-methyl-1-[(4-methyl-2,6,7-trioxabicyclo[2.2.2]oct-1-yl)methyl]-2 -oxo-3-pyrrolidinyl]-4-phenyl-, (4S)-

881422-63-5

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Basic information

Product Name: 2-Oxazolidinone, 3-[(3S)-3-methyl-1-[(4-methyl-2,6,7-trioxabicyclo[2.2.2]oct-1-yl)methyl]-2 -oxo-3-pyrrolidinyl]-4-phenyl-, (4S)-
Synonyms:
CAS NO:881422-63-5
Molecular Formula: C21H26N2O6
Molecular Weight: 402.447
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: 2-Oxazolidinone, 3-[(3S)-3-methyl-1-[(4-methyl-2,6,7-trioxabicyclo[2.2.2]oct-1-yl)methyl]-2 -oxo-3-pyrrolidinyl]-4-phenyl-, (4S)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Oxazolidinone, 3-[(3S)-3-methyl-1-[(4-methyl-2,6,7-trioxabicyclo[2.2.2]oct-1-yl)methyl]-2 -oxo-3-pyrrolidinyl]-4-phenyl-, (4S)-(881422-63-5)
EPA Substance Registry System: 2-Oxazolidinone, 3-[(3S)-3-methyl-1-[(4-methyl-2,6,7-trioxabicyclo[2.2.2]oct-1-yl)methyl]-2 -oxo-3-pyrrolidinyl]-4-phenyl-, (4S)-(881422-63-5)

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: 881422-63-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 881422-63-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,4,2 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 881422-63:
(8*8)+(7*8)+(6*1)+(5*4)+(4*2)+(3*2)+(2*6)+(1*3)=175
175 % 10 = 5
So 881422-63-5 is a valid CAS Registry Number.

881422-63-5Upstream product

74-88-4 methyl iodide

881422-63-5Downstream Products

881422-63-5Relevant academic research and scientific papers

Short stereoselective synthesis of α-substituted γ-lactams

Raghavan, Bhooma,Johnson, Rodney L.

, p. 2151 - 2154 (2006)

A concise, stereoselective synthesis of α-substituted γ-lactams is reported. γ-Lactam scaffolds 2 and 3, possessing an Evans' chiral auxiliary and two types of N substituents, were successfully alkylated with different electrophiles to give α-substituted

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