Cas 743430-89-9,(6-bromo-2,3-dimethoxybenzyl)-[2-(6-fluorobenzo[1,3]dioxol-5-yl)ethyl]carbamic acid methyl ester

743430-89-9

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Basic information

Product Name: (6-bromo-2,3-dimethoxybenzyl)-[2-(6-fluorobenzo[1,3]dioxol-5-yl)ethyl]carbamic acid methyl ester
Synonyms: (6-bromo-2,3-dimethoxybenzyl)-[2-(6-fluorobenzo[1,3]dioxol-5-yl)ethyl]carbamic acid methyl ester
CAS NO:743430-89-9
Molecular Formula:
Molecular Weight: 470.292
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: (6-bromo-2,3-dimethoxybenzyl)-[2-(6-fluorobenzo[1,3]dioxol-5-yl)ethyl]carbamic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (6-bromo-2,3-dimethoxybenzyl)-[2-(6-fluorobenzo[1,3]dioxol-5-yl)ethyl]carbamic acid methyl ester(743430-89-9)
EPA Substance Registry System: (6-bromo-2,3-dimethoxybenzyl)-[2-(6-fluorobenzo[1,3]dioxol-5-yl)ethyl]carbamic acid methyl ester(743430-89-9)

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: 743430-89-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 743430-89-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,3,4,3 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 743430-89:
(8*7)+(7*4)+(6*3)+(5*4)+(4*3)+(3*0)+(2*8)+(1*9)=159
159 % 10 = 9
So 743430-89-9 is a valid CAS Registry Number.

743430-89-9Upstream product

743430-89-9Downstream Products

743430-89-9Relevant academic research and scientific papers

A new approach to isoindoloisoquinolinones. A simple synthesis of nuevamine

Moreau, Anne,Couture, Axel,Deniau, Eric,Grandclaudon, Pierre,Lebrun, Stéphane

, p. 6169 - 6176 (2007/10/03)

A convenient and versatile short step synthesis of isoindoloisoquinolinones, illustrated by the total synthesis of the alkaloid nuevamine 1a, is described. The tetracyclic lactam compounds were obtained by a tactical combination of the Parham procedure for the elaboration of the isoindolinone template and an aryne-mediated cyclization giving rise to the nitrogen containing six-membered heteroring unit.

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