Cas 958261-90-0,(E)-methyl 2-(2-bromo-4,5-dimethoxyphenyl)-3-(4-methoxyphenyl)acrylate

958261-90-0

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Basic information

Product Name: (E)-methyl 2-(2-bromo-4,5-dimethoxyphenyl)-3-(4-methoxyphenyl)acrylate
Synonyms: (E)-methyl 2-(2-bromo-4,5-dimethoxyphenyl)-3-(4-methoxyphenyl)acrylate
CAS NO:958261-90-0
Molecular Formula:
Molecular Weight: 407.261
EINECS: N/A
Product Categories: N/A
Mol File: 958261-90-0.mol
Article Data: 1

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 2-(2-bromo-4,5-dimethoxyphenyl)-3-(4-methoxyphenyl)acrylate(CAS DataBase Reference)
NIST Chemistry Reference: (E)-methyl 2-(2-bromo-4,5-dimethoxyphenyl)-3-(4-methoxyphenyl)acrylate(958261-90-0)
EPA Substance Registry System: (E)-methyl 2-(2-bromo-4,5-dimethoxyphenyl)-3-(4-methoxyphenyl)acrylate(958261-90-0)

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: 958261-90-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 958261-90-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,8,2,6 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 958261-90:
(8*9)+(7*5)+(6*8)+(5*2)+(4*6)+(3*1)+(2*9)+(1*0)=210
210 % 10 = 0
So 958261-90-0 is a valid CAS Registry Number.

958261-90-0Upstream product

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958261-90-0Relevant articles and documents

Synthesis of 13a-methylphenanthroindolizidines using radical cascade cyclization: synthetic studies toward (±)-hypoestestatin 1

Takeuchi, Kosuke,Ishita, Atsuko,Matsuo, Jun-ichi,Ishibashi, Hiroyuki

, p. 11101 - 11107 (2008/02/12)

A radical cascade involving 6-endo cyclization of aryl radicals generated from N-acryloyl-N-(1-methylethenyl)-9-bromophenanthren-10-ylmethylamines, followed by 5-endo-trig cyclization of the resulting α-amidoyl radicals afforded phenanthroindolizidines be

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