Cas 1040735-89-4,(3R,7aR,11aR)-8-methyl-5-oxo-3-phenyl-2,3,5,6,7,7a,10,11-octahydrooxazolo[2,3-j]quinoline

1040735-89-4

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Basic information

Product Name: (3R,7aR,11aR)-8-methyl-5-oxo-3-phenyl-2,3,5,6,7,7a,10,11-octahydrooxazolo[2,3-j]quinoline
Synonyms: (3R,7aR,11aR)-8-methyl-5-oxo-3-phenyl-2,3,5,6,7,7a,10,11-octahydrooxazolo[2,3-j]quinoline
CAS NO:1040735-89-4
Molecular Formula:
Molecular Weight: 283.37
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: (3R,7aR,11aR)-8-methyl-5-oxo-3-phenyl-2,3,5,6,7,7a,10,11-octahydrooxazolo[2,3-j]quinoline(CAS DataBase Reference)
NIST Chemistry Reference: (3R,7aR,11aR)-8-methyl-5-oxo-3-phenyl-2,3,5,6,7,7a,10,11-octahydrooxazolo[2,3-j]quinoline(1040735-89-4)
EPA Substance Registry System: (3R,7aR,11aR)-8-methyl-5-oxo-3-phenyl-2,3,5,6,7,7a,10,11-octahydrooxazolo[2,3-j]quinoline(1040735-89-4)

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: 1040735-89-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1040735-89-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,0,7,3 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1040735-89:
(9*1)+(8*0)+(7*4)+(6*0)+(5*7)+(4*3)+(3*5)+(2*8)+(1*9)=124
124 % 10 = 4
So 1040735-89-4 is a valid CAS Registry Number.

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1040735-89-4Relevant academic research and scientific papers

Biomimetic construction of the hydroquinoline ring system. Diastereodivergent enantioselective synthesis of 2,5-disubstituted cis -decahydroquinolines

Amat, Mercedes,Fabregat, Robert,Griera, Rosa,Florindo, Pedro,Molins, Elies,Bosch, Joan

experimental part, p. 3797 - 3805 (2010/08/20)

Figure presented The straightforward enantioselective construction of the hydroquinoline ring system from 1,5-polycarbonyl derivatives, using (R)-phenyglycinol as a chiral latent form of ammonia, is reported. The process mimics the key steps believed to o

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