Cas 1126669-38-2,tert-butyl (R)-5-ethyl-6-oxo-2,5-diphenyl-5,6-dihydro-1,3,4-oxadiazine-4-carboxylate

1126669-38-2

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Basic information

Product Name: tert-butyl (R)-5-ethyl-6-oxo-2,5-diphenyl-5,6-dihydro-1,3,4-oxadiazine-4-carboxylate
Synonyms: tert-butyl (R)-5-ethyl-6-oxo-2,5-diphenyl-5,6-dihydro-1,3,4-oxadiazine-4-carboxylate
CAS NO:1126669-38-2
Molecular Formula:
Molecular Weight: 380.444
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: tert-butyl (R)-5-ethyl-6-oxo-2,5-diphenyl-5,6-dihydro-1,3,4-oxadiazine-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (R)-5-ethyl-6-oxo-2,5-diphenyl-5,6-dihydro-1,3,4-oxadiazine-4-carboxylate(1126669-38-2)
EPA Substance Registry System: tert-butyl (R)-5-ethyl-6-oxo-2,5-diphenyl-5,6-dihydro-1,3,4-oxadiazine-4-carboxylate(1126669-38-2)

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: 1126669-38-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1126669-38-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,6,6,6 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1126669-38:
(9*1)+(8*1)+(7*2)+(6*6)+(5*6)+(4*6)+(3*9)+(2*3)+(1*8)=162
162 % 10 = 2
So 1126669-38-2 is a valid CAS Registry Number.

1126669-38-2Upstream product

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1126669-38-2Relevant academic research and scientific papers

[4+2] Cycloaddition of ketenes with N-benzoyldiazenes catalyzed by N-heterocyclic carbenes

Huang, Xue-Liang,He, Lin,Shao, Pan-Lin,Ye, Song

, p. 192 - 195 (2009)

(Chemical Equation Presented) Enantioselectivity switch: A catalytic enantioselective [4+2] cycloaddition reaction of alkylarylketenes with N-aryl-N′-benzoyldiazenes or N,N′-dibenzoyldiazenes to give 1,3,4-oxadiazin-6-ones 1 was developed by employing N-h

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