Cas 87633-32-7,2-(3,4-Dimethoxyphenyl)-2a,3,4,5-tetrahydro-3-methyl-7,8-methylendioxy-2H-furo<2,3,4-i,k>isochinolin

87633-32-7

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Basic information

Product Name: 2-(3,4-Dimethoxyphenyl)-2a,3,4,5-tetrahydro-3-methyl-7,8-methylendioxy-2H-furo<2,3,4-i,k>isochinolin
Synonyms:
CAS NO:87633-32-7
Molecular Formula:
Molecular Weight: 355.39
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: 2-(3,4-Dimethoxyphenyl)-2a,3,4,5-tetrahydro-3-methyl-7,8-methylendioxy-2H-furo<2,3,4-i,k>isochinolin(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3,4-Dimethoxyphenyl)-2a,3,4,5-tetrahydro-3-methyl-7,8-methylendioxy-2H-furo<2,3,4-i,k>isochinolin(87633-32-7)
EPA Substance Registry System: 2-(3,4-Dimethoxyphenyl)-2a,3,4,5-tetrahydro-3-methyl-7,8-methylendioxy-2H-furo<2,3,4-i,k>isochinolin(87633-32-7)

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: 87633-32-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 87633-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,3 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87633-32:
(7*8)+(6*7)+(5*6)+(4*3)+(3*3)+(2*3)+(1*2)=157
157 % 10 = 7
So 87633-32-7 is a valid CAS Registry Number.

87633-32-7Upstream product

87633-32-7Downstream Products

87633-33-8 2-(3,4-Dimethoxyphenyl)-3-dimethylamino-6,7-methylendioxy-4-vinyl-dihydrobenzofuran

87633-32-7Relevant academic research and scientific papers

Borane Adducts of Narcotine, Hydrastine and Their Reduction Products

Prior, Silvia,Wiegrebe, Wolfgang

, p. 737 - 746 (1983)

α-Narcotine (3), β-Hydrastine (6) and their reduction products bind BH3 coordinatively at the N atom. α-Narcotinediol (8) when treated with potassium tert.butylate and benzophenone does not yield α-anhydronarcotinediol but leads to a quettamine-like compo

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