Cas 194350-35-1,(5-tert-Butoxycarbonylamino-8-phenyl-dithieno[3,2-b;2',3'-e]pyridin-3-yl)-carbamic acid tert-butyl ester

194350-35-1

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Basic information

Product Name: (5-tert-Butoxycarbonylamino-8-phenyl-dithieno[3,2-b;2',3'-e]pyridin-3-yl)-carbamic acid tert-butyl ester
Synonyms: (5-tert-Butoxycarbonylamino-8-phenyl-dithieno[3,2-b;2',3'-e]pyridin-3-yl)-carbamic acid tert-butyl ester
CAS NO:194350-35-1
Molecular Formula:
Molecular Weight: 497.639
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: (5-tert-Butoxycarbonylamino-8-phenyl-dithieno[3,2-b;2',3'-e]pyridin-3-yl)-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (5-tert-Butoxycarbonylamino-8-phenyl-dithieno[3,2-b;2',3'-e]pyridin-3-yl)-carbamic acid tert-butyl ester(194350-35-1)
EPA Substance Registry System: (5-tert-Butoxycarbonylamino-8-phenyl-dithieno[3,2-b;2',3'-e]pyridin-3-yl)-carbamic acid tert-butyl ester(194350-35-1)

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: 194350-35-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 194350-35-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,3,5 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 194350-35:
(8*1)+(7*9)+(6*4)+(5*3)+(4*5)+(3*0)+(2*3)+(1*5)=141
141 % 10 = 1
So 194350-35-1 is a valid CAS Registry Number.

194350-35-1Upstream product

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194350-35-1Relevant academic research and scientific papers

Synthesis and reactivity of alkyl (4-aminothien-3-yl)carbamates

Brugier, Delphine,Outurquin, Francis,Paulmier, Claude

, p. 10331 - 10344 (2007/10/03)

Monocarbamates 2 have been prepared from 3,4-diaminothiophene 1 and were alkylated on the thiophene nucleus using an aldehyde and selenophenol, under acid catalysis. This reaction has allowed the access to 2-alkyl 3,4-diaminothiophenes 9, 3,5-diaminodithieno[3,2-b:2',3'-e]pyridines 10 and 1-alkyl thieno[3,4-d]imidazolones 13.

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