Cas 879290-18-3,5H-Isoxazolo[3,2-a]isoquinoline-1,2-dicarboxylic acid, 6,10b-dihydro-8,9-dimethoxy-10b-phenyl-, dimethyl ester

879290-18-3

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Basic information

Product Name: 5H-Isoxazolo[3,2-a]isoquinoline-1,2-dicarboxylic acid, 6,10b-dihydro-8,9-dimethoxy-10b-phenyl-, dimethyl ester
Synonyms:
CAS NO:879290-18-3
Molecular Formula: C23H23NO7
Molecular Weight: 425.438
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: 5H-Isoxazolo[3,2-a]isoquinoline-1,2-dicarboxylic acid, 6,10b-dihydro-8,9-dimethoxy-10b-phenyl-, dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5H-Isoxazolo[3,2-a]isoquinoline-1,2-dicarboxylic acid, 6,10b-dihydro-8,9-dimethoxy-10b-phenyl-, dimethyl ester(879290-18-3)
EPA Substance Registry System: 5H-Isoxazolo[3,2-a]isoquinoline-1,2-dicarboxylic acid, 6,10b-dihydro-8,9-dimethoxy-10b-phenyl-, dimethyl ester(879290-18-3)

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: 879290-18-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 879290-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,2,9 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 879290-18:
(8*8)+(7*7)+(6*9)+(5*2)+(4*9)+(3*0)+(2*1)+(1*8)=223
223 % 10 = 3
So 879290-18-3 is a valid CAS Registry Number.

879290-18-3Upstream product

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879290-18-3Relevant academic research and scientific papers

Synthesis of stable azomethine ylides by the rearrangement of 1,3-dipolar cycloadducts of 3,4-dihydroisoquinoline-2-oxides with DMAD

Co?kun, Necdet,Tun?man, Selen

, p. 1345 - 1350 (2007/10/03)

1-Aryl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolines were prepared according to a one-pot procedure involving the reaction of 2-(3,4- dimethoxyphenyl)-ethylamine with aromatic aldehydes in TFA at reflux. The tetrahydroisoquinolines were treated with Hsub

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