Cas 916085-19-3,N-{1-(3-hydroxypropyl)-2-[(trimethylsilyl)methyl]-2-cyclopenten-1-yl}-4-methylbenzenesulfonamide

916085-19-3

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Basic information

Product Name: N-{1-(3-hydroxypropyl)-2-[(trimethylsilyl)methyl]-2-cyclopenten-1-yl}-4-methylbenzenesulfonamide
Synonyms: N-{1-(3-hydroxypropyl)-2-[(trimethylsilyl)methyl]-2-cyclopenten-1-yl}-4-methylbenzenesulfonamide
CAS NO:916085-19-3
Molecular Formula:
Molecular Weight: 381.612
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-{1-(3-hydroxypropyl)-2-[(trimethylsilyl)methyl]-2-cyclopenten-1-yl}-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-{1-(3-hydroxypropyl)-2-[(trimethylsilyl)methyl]-2-cyclopenten-1-yl}-4-methylbenzenesulfonamide(916085-19-3)
EPA Substance Registry System: N-{1-(3-hydroxypropyl)-2-[(trimethylsilyl)methyl]-2-cyclopenten-1-yl}-4-methylbenzenesulfonamide(916085-19-3)

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: 916085-19-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 916085-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,0,8 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 916085-19:
(8*9)+(7*1)+(6*6)+(5*0)+(4*8)+(3*5)+(2*1)+(1*9)=173
173 % 10 = 3
So 916085-19-3 is a valid CAS Registry Number.

916085-19-3Upstream product

916085-19-3Downstream Products

916085-19-3Relevant academic research and scientific papers

New route to azaspirocycles via the organolithium-mediated conversion of β-alkoxy aziridines into cyclopentenyl amines

Moore, Stephen P.,Coote, Susannah C.,O'Brien, Peter,Gilday, John

, p. 5145 - 5148 (2007/10/03)

(Chemical Equation Presented) A new three-step route to azaspirocycles involving the organolithium-mediated conversion of β-alkoxy aziridines into substituted cyclopentenyl amines, hydroboration, and cyclization has been developed. The methodology is util

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