Cas 898828-47-2,N-(6-bromo-4-isopropoxy-2-methoxy-3-methylbenzyl)-N-(2,2-dimethoxyethylidene)amine

898828-47-2

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Basic information

Product Name: N-(6-bromo-4-isopropoxy-2-methoxy-3-methylbenzyl)-N-(2,2-dimethoxyethylidene)amine
Synonyms: N-(6-bromo-4-isopropoxy-2-methoxy-3-methylbenzyl)-N-(2,2-dimethoxyethylidene)amine
CAS NO:898828-47-2
Molecular Formula:
Molecular Weight: 376.291
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: N-(6-bromo-4-isopropoxy-2-methoxy-3-methylbenzyl)-N-(2,2-dimethoxyethylidene)amine(CAS DataBase Reference)
NIST Chemistry Reference: N-(6-bromo-4-isopropoxy-2-methoxy-3-methylbenzyl)-N-(2,2-dimethoxyethylidene)amine(898828-47-2)
EPA Substance Registry System: N-(6-bromo-4-isopropoxy-2-methoxy-3-methylbenzyl)-N-(2,2-dimethoxyethylidene)amine(898828-47-2)

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: 898828-47-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 898828-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,8,2 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 898828-47:
(8*8)+(7*9)+(6*8)+(5*8)+(4*2)+(3*8)+(2*4)+(1*7)=262
262 % 10 = 2
So 898828-47-2 is a valid CAS Registry Number.

898828-47-2Upstream product

863647-50-1 6-bromo-4-isopropoxy-2-methoxy-3-methylbenzaldehyde

898828-47-2Downstream Products

898828-45-0 methyl N-(6-bromo-4-isopropoxy-2-methoxy-3-methylbenzyl)-N-(2,2-dimethoxyethyl)carbamate

898828-47-2Relevant academic research and scientific papers

A new synthesis of the phytotoxin porritoxin

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

, p. 5787 - 5790 (2006)

A convenient synthesis of the phytotoxin porritoxin is described. Central to the approach employed is the formation of the isoindolinone template obtained via a directed lithiation/Parham cyclization process enabling the concomitant connection of an aceta

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