Cas 99563-65-2,(4-Bromo-phenyl)-(4-phenyl-5-{[1-pyrrolidin-1-yl-meth-(E)-ylidene]-amino}-thiophen-2-yl)-methanone

99563-65-2

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Basic information

Product Name: (4-Bromo-phenyl)-(4-phenyl-5-{[1-pyrrolidin-1-yl-meth-(E)-ylidene]-amino}-thiophen-2-yl)-methanone
Synonyms:
CAS NO:99563-65-2
Molecular Formula:
Molecular Weight: 439.376
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: (4-Bromo-phenyl)-(4-phenyl-5-{[1-pyrrolidin-1-yl-meth-(E)-ylidene]-amino}-thiophen-2-yl)-methanone(CAS DataBase Reference)
NIST Chemistry Reference: (4-Bromo-phenyl)-(4-phenyl-5-{[1-pyrrolidin-1-yl-meth-(E)-ylidene]-amino}-thiophen-2-yl)-methanone(99563-65-2)
EPA Substance Registry System: (4-Bromo-phenyl)-(4-phenyl-5-{[1-pyrrolidin-1-yl-meth-(E)-ylidene]-amino}-thiophen-2-yl)-methanone(99563-65-2)

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: 99563-65-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 99563-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,5,6 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 99563-65:
(7*9)+(6*9)+(5*5)+(4*6)+(3*3)+(2*6)+(1*5)=192
192 % 10 = 2
So 99563-65-2 is a valid CAS Registry Number.

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99563-65-2Relevant academic research and scientific papers

Formylation Products of Thioamides. XIV, Synthesis of Substituted Thiazoles and Thiophenes by the Reaction of N,N'-Bis(aminomethylidene)thioureas or N-(3-Aminothioacryloyl)-formamidines with Alkylating Reagents

Knoll, Alexander,Liebscher, Juergen,Radeglia, Reiner

, p. 463 - 470 (2007/10/02)

N,N'-Bis(aminomethylidene)thioureas 1 react with electron acceptor substituted methyl halides 2 under the formation of 2-formamidinothiazoles 4.The reaction of N-(3-aminothioacryloyl)-formamidines 5 with substituted methyl halides 2 gives either 2-formami

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