Cas 1140907-82-9,N-[rac-(tert-butyldimethylsilanyloxy)-2-(5-ethylfuran-2-yl)ethyl]-4-methylphenylsulfonamide

1140907-82-9

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Basic information

Product Name: N-[rac-(tert-butyldimethylsilanyloxy)-2-(5-ethylfuran-2-yl)ethyl]-4-methylphenylsulfonamide
Synonyms: N-[rac-(tert-butyldimethylsilanyloxy)-2-(5-ethylfuran-2-yl)ethyl]-4-methylphenylsulfonamide
CAS NO:1140907-82-9
Molecular Formula:
Molecular Weight: 423.649
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: N-[rac-(tert-butyldimethylsilanyloxy)-2-(5-ethylfuran-2-yl)ethyl]-4-methylphenylsulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[rac-(tert-butyldimethylsilanyloxy)-2-(5-ethylfuran-2-yl)ethyl]-4-methylphenylsulfonamide(1140907-82-9)
EPA Substance Registry System: N-[rac-(tert-butyldimethylsilanyloxy)-2-(5-ethylfuran-2-yl)ethyl]-4-methylphenylsulfonamide(1140907-82-9)

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: 1140907-82-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1140907-82-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,0,9,0 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1140907-82:
(9*1)+(8*1)+(7*4)+(6*0)+(5*9)+(4*0)+(3*7)+(2*8)+(1*2)=129
129 % 10 = 9
So 1140907-82-9 is a valid CAS Registry Number.

1140907-82-9Upstream product

98-59-9 p-toluenesulfonyl chloride

1140907-82-9Downstream Products

1140907-83-0 rac-N-[2-(tert-butyldimethylsilanyloxy)-2-(5-ethylfuran-2-ylethyl)ethyl]-4-methyl-N-prop-2-ynylphenylsulfonamide

1140907-82-9Relevant academic research and scientific papers

Enantiomerically pure tetrahydroisoquinolines by enzyme catalysis and gold-catalyzed phenol synthesis

Hashmi, A. Stephen K.,Ata, Filiz,Haufe, Patrick,Rominger, Frank

body text, p. 1919 - 1927 (2009/06/20)

Five different furfural derivatives were converted to chiral cyanohydrins by enzyme catalysis in good enantiomeric excess. After a sequence of silyl protection, nitrile reduction, tosylation and propargylation, substrates for the gold(I) catalyzed cyclois

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