Cas 858765-63-6,1-(4-METHOXY-6-METHYL-5,6,7,8-TETRAHYDRO-[1,3]DIOXOLO[4,5-G]ISOQUINOLIN-5-YL)-PENTANE-2,4-DIONE

858765-63-6

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Basic information

Product Name: 1-(4-METHOXY-6-METHYL-5,6,7,8-TETRAHYDRO-[1,3]DIOXOLO[4,5-G]ISOQUINOLIN-5-YL)-PENTANE-2,4-DIONE
Synonyms: 1-(4-METHOXY-6-METHYL-5,6,7,8-TETRAHYDRO-[1,3]DIOXOLO[4,5-G]ISOQUINOLIN-5-YL)-PENTANE-2,4-DIONE
CAS NO:858765-63-6
Molecular Formula: C17H21NO5
Molecular Weight: 319.35234
EINECS: N/A
Product Categories: N/A
Mol File: 858765-63-6.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-(4-METHOXY-6-METHYL-5,6,7,8-TETRAHYDRO-[1,3]DIOXOLO[4,5-G]ISOQUINOLIN-5-YL)-PENTANE-2,4-DIONE(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-METHOXY-6-METHYL-5,6,7,8-TETRAHYDRO-[1,3]DIOXOLO[4,5-G]ISOQUINOLIN-5-YL)-PENTANE-2,4-DIONE(858765-63-6)
EPA Substance Registry System: 1-(4-METHOXY-6-METHYL-5,6,7,8-TETRAHYDRO-[1,3]DIOXOLO[4,5-G]ISOQUINOLIN-5-YL)-PENTANE-2,4-DIONE(858765-63-6)

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: 858765-63-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 858765-63-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,8,7,6 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 858765-63:
(8*8)+(7*5)+(6*8)+(5*7)+(4*6)+(3*5)+(2*6)+(1*3)=236
236 % 10 = 6
So 858765-63-6 is a valid CAS Registry Number.

858765-63-6Upstream product

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858765-63-6Relevant academic research and scientific papers

Chemical modification of plant alkaloids. 4. Reaction of cotarnine with bifunctional NH- and CH-acids

Krasnov,Kartsev,Vasilevskii

, p. 446 - 450 (2005)

1-Substituted 1,2,3,4-tetrahydroisoquinoline systems were prepared by reaction of cotarnine with the NH-and CH-acids methyl- and acyl derivatives of pyrazole and 1,3-dicarbonyl reagents. Depending on the structure and reaction conditions, bifunctional pyrazole nucleophiles can give substitution products at the N atom, methyl, or acyl group; 1,3-diketones, at the terminal methyl. Rearrangements occurring during the reaction of cotarnine with bifunctional substrates were studied. 2005 Springer Science+Business Media, Inc.

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