Cas 699432-69-4,(2S,3aS,6S)-6-tert-butyl-2-(4'-tert-butylphenyl)-5-methyl-tetrahydroimidazo[1,5-b]isoxazol-4-one

699432-69-4

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Basic information

Product Name: (2S,3aS,6S)-6-tert-butyl-2-(4'-tert-butylphenyl)-5-methyl-tetrahydroimidazo[1,5-b]isoxazol-4-one
Synonyms: (2S,3aS,6S)-6-tert-butyl-2-(4'-tert-butylphenyl)-5-methyl-tetrahydroimidazo[1,5-b]isoxazol-4-one
CAS NO:699432-69-4
Molecular Formula:
Molecular Weight: 330.47
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,3aS,6S)-6-tert-butyl-2-(4'-tert-butylphenyl)-5-methyl-tetrahydroimidazo[1,5-b]isoxazol-4-one(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3aS,6S)-6-tert-butyl-2-(4'-tert-butylphenyl)-5-methyl-tetrahydroimidazo[1,5-b]isoxazol-4-one(699432-69-4)
EPA Substance Registry System: (2S,3aS,6S)-6-tert-butyl-2-(4'-tert-butylphenyl)-5-methyl-tetrahydroimidazo[1,5-b]isoxazol-4-one(699432-69-4)

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: 699432-69-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 699432-69-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,9,4,3 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 699432-69:
(8*6)+(7*9)+(6*9)+(5*4)+(4*3)+(3*2)+(2*6)+(1*9)=224
224 % 10 = 4
So 699432-69-4 is a valid CAS Registry Number.

699432-69-4Upstream product

101143-56-0 (2R)-2-(tert-butyl)-3-methylimidazolidin-4-one

699432-69-4Downstream Products

699432-69-4Relevant academic research and scientific papers

2-tert-butyl-3-methyl-2,3-dihydroimidazol-4-one-N-oxide: A new nitrone-based chiral glycine equivalent

Baldwin, Steven W.,Long, Alan

, p. 1653 - 1656 (2004)

Cycloaddition reactions between a new homochiral imidazolone-derived nitrone afford cycloadducts in high yield and with high stereoselectivity. Subsequent cycloadduct elaboration affords the γ-lactones of γ-hydroxy-α-amino acids as well as the optically pure amino acids themselves.

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