Cas 675876-33-2,1H-Pyrrole-2-acetamide, 1-[(2-nitrophenyl)sulfonyl]-a-[(1-oxo-2-propynyl)(phenylmethyl)amino]-N- (phenylmethyl)-

675876-33-2

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Basic information

Product Name: 1H-Pyrrole-2-acetamide, 1-[(2-nitrophenyl)sulfonyl]-a-[(1-oxo-2-propynyl)(phenylmethyl)amino]-N- (phenylmethyl)-
Synonyms:
CAS NO:675876-33-2
Molecular Formula: C29H24N4O6S
Molecular Weight: 556.599
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: 1H-Pyrrole-2-acetamide, 1-[(2-nitrophenyl)sulfonyl]-a-[(1-oxo-2-propynyl)(phenylmethyl)amino]-N- (phenylmethyl)-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Pyrrole-2-acetamide, 1-[(2-nitrophenyl)sulfonyl]-a-[(1-oxo-2-propynyl)(phenylmethyl)amino]-N- (phenylmethyl)-(675876-33-2)
EPA Substance Registry System: 1H-Pyrrole-2-acetamide, 1-[(2-nitrophenyl)sulfonyl]-a-[(1-oxo-2-propynyl)(phenylmethyl)amino]-N- (phenylmethyl)-(675876-33-2)

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: 675876-33-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 675876-33-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,5,8,7 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 675876-33:
(8*6)+(7*7)+(6*5)+(5*8)+(4*7)+(3*6)+(2*3)+(1*3)=222
222 % 10 = 2
So 675876-33-2 is a valid CAS Registry Number.

675876-33-2Upstream product

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675876-33-2Relevant academic research and scientific papers

An Atom-Economical Approach to Conformationally Constrained Tricyclic Nitrogen Heterocycles via Sequential and Tandem Ugi/Intramolecular Diels-Alder Reaction of Pyrrole

Paulvannan

, p. 1207 - 1214 (2007/10/03)

An efficient approach to rigid tricyclic nitrogen heterocycles via sequential and tandem Ugi/intramolecular Diels-Alder (IMDA) cycloaddition of pyrrole is described. The one-pot Ugi four-component condensation (4CC) reaction was used as the key transforma

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