Cas 308803-66-9,(E)-methyl N-[2-(4,5-dimethoxy-2-[2-(4-methoxyphenyl)ethenyl]phenyl)ethyl]-N-methylcarbamate

308803-66-9

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Basic information

Product Name: (E)-methyl N-[2-(4,5-dimethoxy-2-[2-(4-methoxyphenyl)ethenyl]phenyl)ethyl]-N-methylcarbamate
Synonyms: (E)-methyl N-[2-(4,5-dimethoxy-2-[2-(4-methoxyphenyl)ethenyl]phenyl)ethyl]-N-methylcarbamate
CAS NO:308803-66-9
Molecular Formula:
Molecular Weight: 385.46
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: (E)-methyl N-[2-(4,5-dimethoxy-2-[2-(4-methoxyphenyl)ethenyl]phenyl)ethyl]-N-methylcarbamate(CAS DataBase Reference)
NIST Chemistry Reference: (E)-methyl N-[2-(4,5-dimethoxy-2-[2-(4-methoxyphenyl)ethenyl]phenyl)ethyl]-N-methylcarbamate(308803-66-9)
EPA Substance Registry System: (E)-methyl N-[2-(4,5-dimethoxy-2-[2-(4-methoxyphenyl)ethenyl]phenyl)ethyl]-N-methylcarbamate(308803-66-9)

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: 308803-66-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 308803-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,8,8,0 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 308803-66:
(8*3)+(7*0)+(6*8)+(5*8)+(4*0)+(3*3)+(2*6)+(1*6)=139
139 % 10 = 9
So 308803-66-9 is a valid CAS Registry Number.

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308803-66-9Relevant academic research and scientific papers

Syntheses of the seco benzyltetrahydroisoquinoline alkaloids polysignine and methoxypolysignine

Nimgirawath, Surachai

, p. 523 - 525 (2000)

The structures previously assigned to the seco benzyltetrahydroisoquinoline alkaloids polysignine (1) and methoxypolysignine (2) have been confirmed by total syntheses in which the key step involved cleavage of the C 1-N bonds in the corresponding N-methylbenzyltetrahydroisoquinolines. CSIRO 2000.

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