Cas 660414-69-7,Bicyclo[4.2.0]octa-1,3,5-triene-7-carbonitrile, 7-[2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-3-[[tris(1-methylethyl)silyl]oxy]-

660414-69-7

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Basic information

Product Name: Bicyclo[4.2.0]octa-1,3,5-triene-7-carbonitrile, 7-[2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-3-[[tris(1-methylethyl)silyl]oxy]-
Synonyms:
CAS NO:660414-69-7
Molecular Formula: C25H39NO3Si
Molecular Weight: 429.675
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: Bicyclo[4.2.0]octa-1,3,5-triene-7-carbonitrile, 7-[2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-3-[[tris(1-methylethyl)silyl]oxy]-(CAS DataBase Reference)
NIST Chemistry Reference: Bicyclo[4.2.0]octa-1,3,5-triene-7-carbonitrile, 7-[2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-3-[[tris(1-methylethyl)silyl]oxy]-(660414-69-7)
EPA Substance Registry System: Bicyclo[4.2.0]octa-1,3,5-triene-7-carbonitrile, 7-[2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]-3-[[tris(1-methylethyl)silyl]oxy]-(660414-69-7)

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: 660414-69-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 660414-69-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,0,4,1 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 660414-69:
(8*6)+(7*6)+(6*0)+(5*4)+(4*1)+(3*4)+(2*6)+(1*9)=147
147 % 10 = 7
So 660414-69-7 is a valid CAS Registry Number.

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660414-69-7Relevant academic research and scientific papers

Synthesis of new potentially antiviral furan-fused compounds by thermolysis of benzocyclobutene derivatives

Matsuya, Yuji,Qin, Hongbo,Nagaoka, Mamiko,Nemoto, Hideo

, p. 207 - 211 (2007/10/03)

New potentially antiviral furan-fused tetracyclic compounds were prepared using intramolecular cycloaddition of o-quinodimethane generated by thermolysis of benzocyclobutene derivatives. It was found that the reaction course was changed depending on the length of alkyl chain connecting quinodimethane and furan ring.

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