Cas 602302-21-6,(3R,5aS,9aS,10aS)-6-methoxy-5a-(methoxycarbonyl)-5-oxo-3-phenyl-8-(triisopropylsilyloxy)-2,3,9,9a,10,10a-hexahydro-6H-oxazolo[3,2-b]isoquinoline

602302-21-6

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Basic information

Product Name: (3R,5aS,9aS,10aS)-6-methoxy-5a-(methoxycarbonyl)-5-oxo-3-phenyl-8-(triisopropylsilyloxy)-2,3,9,9a,10,10a-hexahydro-6H-oxazolo[3,2-b]isoquinoline
Synonyms: (3R,5aS,9aS,10aS)-6-methoxy-5a-(methoxycarbonyl)-5-oxo-3-phenyl-8-(triisopropylsilyloxy)-2,3,9,9a,10,10a-hexahydro-6H-oxazolo[3,2-b]isoquinoline
CAS NO:602302-21-6
Molecular Formula:
Molecular Weight: 529.749
EINECS: N/A
Product Categories: N/A
Mol File: 602302-21-6.mol
Article Data: 1

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: (3R,5aS,9aS,10aS)-6-methoxy-5a-(methoxycarbonyl)-5-oxo-3-phenyl-8-(triisopropylsilyloxy)-2,3,9,9a,10,10a-hexahydro-6H-oxazolo[3,2-b]isoquinoline(CAS DataBase Reference)
NIST Chemistry Reference: (3R,5aS,9aS,10aS)-6-methoxy-5a-(methoxycarbonyl)-5-oxo-3-phenyl-8-(triisopropylsilyloxy)-2,3,9,9a,10,10a-hexahydro-6H-oxazolo[3,2-b]isoquinoline(602302-21-6)
EPA Substance Registry System: (3R,5aS,9aS,10aS)-6-methoxy-5a-(methoxycarbonyl)-5-oxo-3-phenyl-8-(triisopropylsilyloxy)-2,3,9,9a,10,10a-hexahydro-6H-oxazolo[3,2-b]isoquinoline(602302-21-6)

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: 602302-21-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 602302-21-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,2,3,0 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 602302-21:
(8*6)+(7*0)+(6*2)+(5*3)+(4*0)+(3*2)+(2*2)+(1*1)=86
86 % 10 = 6
So 602302-21-6 is a valid CAS Registry Number.

602302-21-6Upstream product

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602302-21-6Relevant articles and documents

Diels-Alder reactions of phenylglycinol-derived bicyclic lactams. Enantiodivergent synthesis of cis-hydroisoquinolines

Casamitjana, Nuria,Amat, Mercedes,Llor, Nuria,Carreras, Marcal,Pujol, Xavier,Fernandez, M. Montserrat,Lopez, Virgina,Molins, Elies,Miravitlles, Carles,Bosch, Joan

, p. 2033 - 2039 (2007/10/03)

The diastereomeric phenylglycinol-derived unsaturated δ-lactams trans-3 and cis-3 react with dienes with exo facial diastereoselectivity to give the corresponding tricyclic adducts, which were ultimately converted to enantiomeric cis-hydroisoquinolines.

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