Cas 1275622-27-9,methyl 7a-(4-dimethylaminophenyl)-2,2,3,3-tetramethyl-6-phenyl-1,2,3,7a-tetrahydroimidazo[1,2-b]isoxazole-7-carboxylate

1275622-27-9

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Basic information

Product Name: methyl 7a-(4-dimethylaminophenyl)-2,2,3,3-tetramethyl-6-phenyl-1,2,3,7a-tetrahydroimidazo[1,2-b]isoxazole-7-carboxylate
Synonyms:
CAS NO:1275622-27-9
Molecular Formula:
Molecular Weight: 421.539
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: methyl 7a-(4-dimethylaminophenyl)-2,2,3,3-tetramethyl-6-phenyl-1,2,3,7a-tetrahydroimidazo[1,2-b]isoxazole-7-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 7a-(4-dimethylaminophenyl)-2,2,3,3-tetramethyl-6-phenyl-1,2,3,7a-tetrahydroimidazo[1,2-b]isoxazole-7-carboxylate(1275622-27-9)
EPA Substance Registry System: methyl 7a-(4-dimethylaminophenyl)-2,2,3,3-tetramethyl-6-phenyl-1,2,3,7a-tetrahydroimidazo[1,2-b]isoxazole-7-carboxylate(1275622-27-9)

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: 1275622-27-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1275622-27-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,5,6,2 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1275622-27:
(9*1)+(8*2)+(7*7)+(6*5)+(5*6)+(4*2)+(3*2)+(2*2)+(1*7)=159
159 % 10 = 9
So 1275622-27-9 is a valid CAS Registry Number.

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1275622-27-9Relevant academic research and scientific papers

Mechanism of the migration of the substituent in 1,2,3,7a- tetrahydroimidazo[1,2-b]isoxazole derivatives

Chukanov,Popov,Drebushchak,Reznikov

experimental part, p. 1817 - 1826 (2011/05/07)

The thermolysis of 1,2,3,7a-tetrahydroimidazo[1,2-b]isoxazole derivatives results in intramolecular rearrangements by two main pathways. One rearrangement affords azomethine ylide derivatives. Another rearrangement leads to the migration of the substituen

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