Cas 1404471-91-5,1-(2-bromo-4,5-dimethoxybenzoyl)-N-(tert-butyl)-2-(4-chlorophenyl)-2,3-dihydro-1H-pyrrole-2-carboxamide

1404471-91-5

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Basic information

Product Name: 1-(2-bromo-4,5-dimethoxybenzoyl)-N-(tert-butyl)-2-(4-chlorophenyl)-2,3-dihydro-1H-pyrrole-2-carboxamide
Synonyms: 1-(2-bromo-4,5-dimethoxybenzoyl)-N-(tert-butyl)-2-(4-chlorophenyl)-2,3-dihydro-1H-pyrrole-2-carboxamide
CAS NO:1404471-91-5
Molecular Formula:
Molecular Weight: 521.838
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: 1-(2-bromo-4,5-dimethoxybenzoyl)-N-(tert-butyl)-2-(4-chlorophenyl)-2,3-dihydro-1H-pyrrole-2-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-bromo-4,5-dimethoxybenzoyl)-N-(tert-butyl)-2-(4-chlorophenyl)-2,3-dihydro-1H-pyrrole-2-carboxamide(1404471-91-5)
EPA Substance Registry System: 1-(2-bromo-4,5-dimethoxybenzoyl)-N-(tert-butyl)-2-(4-chlorophenyl)-2,3-dihydro-1H-pyrrole-2-carboxamide(1404471-91-5)

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: 1404471-91-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1404471-91-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,4,4,7 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1404471-91:
(9*1)+(8*4)+(7*0)+(6*4)+(5*4)+(4*7)+(3*1)+(2*9)+(1*1)=135
135 % 10 = 5
So 1404471-91-5 is a valid CAS Registry Number.

1404471-91-5Upstream product

1404471-91-5Downstream Products

1404471-91-5Relevant academic research and scientific papers

Two-step synthesis of 2,3-dihydropyrroles via a formal 5-endo cycloisomerization of Ugi 4-CR/propargyl adducts

Polindara-Garcia, Luis A.,Miranda, Luis D.

supporting information, p. 5408 - 5411,4 (2012/12/12)

A practical two-step synthesis of 2,3-dihydropyrroles from Ugi 4-CR/propargyl adducts is presented. The protocol includes a base-mediated formation of an allenamide functional group and an in situ metal-free formal 5-endo cycloisomerization that occurs in a highly regioselective manner at the allenamide C-γ.

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