Cas 504422-12-2,[3-(4-fluoro-phenyl)-2-(4-methylsulfanyl-phenyl)-benzofuran-5-yl]-carbamic acid <i>tert</i>-butyl ester

504422-12-2

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Basic information

Product Name: [3-(4-fluoro-phenyl)-2-(4-methylsulfanyl-phenyl)-benzofuran-5-yl]-carbamic acid tert-butyl ester
Synonyms: [3-(4-fluoro-phenyl)-2-(4-methylsulfanyl-phenyl)-benzofuran-5-yl]-carbamic acid tert-butyl ester
CAS NO:504422-12-2
Molecular Formula:
Molecular Weight: 449.546
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: [3-(4-fluoro-phenyl)-2-(4-methylsulfanyl-phenyl)-benzofuran-5-yl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [3-(4-fluoro-phenyl)-2-(4-methylsulfanyl-phenyl)-benzofuran-5-yl]-carbamic acid tert-butyl ester(504422-12-2)
EPA Substance Registry System: [3-(4-fluoro-phenyl)-2-(4-methylsulfanyl-phenyl)-benzofuran-5-yl]-carbamic acid tert-butyl ester(504422-12-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 504422-12-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 504422-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,4,4,2 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 504422-12:
(8*5)+(7*0)+(6*4)+(5*4)+(4*2)+(3*2)+(2*1)+(1*2)=102
102 % 10 = 2
So 504422-12-2 is a valid CAS Registry Number.

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504422-12-2Downstream Products

504422-12-2Relevant academic research and scientific papers

Chemistry of aminophenols. Part 3: First synthesis of nitrobenzo[b]furans via a coupling-cyclization approach

Dai, Wei-Min,Lai, Kwong Wah

, p. 9377 - 9380 (2007/10/03)

The first synthesis of 4-, 5-, and 6-nitrobenzo[b]furans has been achieved via the Sonogashira cross-coupling reaction of 2-iodonitrophenol acetates prepared from commercially available and inexpensive 2-aminonitrophenols. The obtained 2-alkynylnitropheno

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