Cas 139210-92-7,5,6,11,12-Naphthacenetetrone, 1-(2-furanyl)-1,4,4a,12a-tetrahydro-3-[(trimethylsilyl)oxy]-

139210-92-7

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Basic information

Product Name: 5,6,11,12-Naphthacenetetrone, 1-(2-furanyl)-1,4,4a,12a-tetrahydro-3-[(trimethylsilyl)oxy]-
Synonyms:
CAS NO:139210-92-7
Molecular Formula: C25H22O6Si
Molecular Weight:
EINECS: N/A
Product Categories: N/A
Mol File: 139210-92-7.mol
Article Data: 1

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: 5,6,11,12-Naphthacenetetrone, 1-(2-furanyl)-1,4,4a,12a-tetrahydro-3-[(trimethylsilyl)oxy]-(CAS DataBase Reference)
NIST Chemistry Reference: 5,6,11,12-Naphthacenetetrone, 1-(2-furanyl)-1,4,4a,12a-tetrahydro-3-[(trimethylsilyl)oxy]-(139210-92-7)
EPA Substance Registry System: 5,6,11,12-Naphthacenetetrone, 1-(2-furanyl)-1,4,4a,12a-tetrahydro-3-[(trimethylsilyl)oxy]-(139210-92-7)

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
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Hazardous Substances Data: 139210-92-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 139210-92-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,2,1 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 139210-92:
(8*1)+(7*3)+(6*9)+(5*2)+(4*1)+(3*0)+(2*9)+(1*2)=117
117 % 10 = 7
So 139210-92-7 is a valid CAS Registry Number.

139210-92-7Upstream product

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139210-92-7Relevant articles and documents

PRODUCTION OF 2-FURYLCYCLANONES BY DIENE SYNTHESIS

Tolstikov, G. A.,Shul'ts, E.E.,Safarova, G.M.,Spirikhin, L.V.,Panasenko, A.A.

, p. 1110 - 1119 (2007/10/02)

The diene synthesis reaction with the new highly active dienes 1-(2-furyl)- and (5-methyl-2-furyl)-3-trimethylsilyloxybutadienes and various dienophiles is a convenient method for the production of 2-furylcyclanones.It was established that the cycloaddition of the above-mentioned dienes to unsymmetrical dienophiles is highly regioselective.

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