Cas 1611486-21-5,ethyl 2-[benzamido(2-(2-formylthiophen-3-yl)phenyl)methyl]acrylate

1611486-21-5

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Basic information

Product Name: ethyl 2-[benzamido(2-(2-formylthiophen-3-yl)phenyl)methyl]acrylate
Synonyms: ethyl 2-[benzamido(2-(2-formylthiophen-3-yl)phenyl)methyl]acrylate
CAS NO:1611486-21-5
Molecular Formula:
Molecular Weight: 419.501
EINECS: N/A
Product Categories: N/A
Mol File: 1611486-21-5.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: ethyl 2-[benzamido(2-(2-formylthiophen-3-yl)phenyl)methyl]acrylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2-[benzamido(2-(2-formylthiophen-3-yl)phenyl)methyl]acrylate(1611486-21-5)
EPA Substance Registry System: ethyl 2-[benzamido(2-(2-formylthiophen-3-yl)phenyl)methyl]acrylate(1611486-21-5)

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: 1611486-21-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1611486-21-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,1,4,8 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1611486-21:
(9*1)+(8*6)+(7*1)+(6*1)+(5*4)+(4*8)+(3*6)+(2*2)+(1*1)=145
145 % 10 = 5
So 1611486-21-5 is a valid CAS Registry Number.

1611486-21-5Upstream product

4347-31-3 2-formylthiophene-3-boronic acid

1611486-21-5Downstream Products

1611486-21-5Relevant articles and documents

An alternate route to substituted 6,7-dihydro 5H-dibenz[c,e]azepines from allylbenzamides derived from the Morita-Baylis-Hillman adducts

Bhowmik, Subhendu,Bhattacharyya, Soumya,Batra, Sanjay

, p. 4031 - 4037 (2014/06/09)

An acid-catalyzed modular synthesis of substituted 5H-dibenz[c,e]azepines from a biaryl allylbenzamides prepared from the MBH adducts via a cascade dearoylation and intramolecular cyclization is described. The utility of the product for preparing 7,9-dihydro-4bH-dibenz[c,e]pyrrolo[1,2-a]azepine is also presented.

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