Cas 471241-75-5,2-[4-(<i>tert</i>-butyl-diphenyl-silanyloxymethyl)-2-oxo-hexahydro-furo[3,4-<i>b</i>]furan-6-yloxy]-isoindole-1,3-dione

471241-75-5

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Basic information

Product Name: 2-[4-(tert-butyl-diphenyl-silanyloxymethyl)-2-oxo-hexahydro-furo[3,4-b]furan-6-yloxy]-isoindole-1,3-dione
Synonyms:
CAS NO:471241-75-5
Molecular Formula:
Molecular Weight: 557.675
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: 2-[4-(tert-butyl-diphenyl-silanyloxymethyl)-2-oxo-hexahydro-furo[3,4-b]furan-6-yloxy]-isoindole-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: 2-[4-(tert-butyl-diphenyl-silanyloxymethyl)-2-oxo-hexahydro-furo[3,4-b]furan-6-yloxy]-isoindole-1,3-dione(471241-75-5)
EPA Substance Registry System: 2-[4-(tert-butyl-diphenyl-silanyloxymethyl)-2-oxo-hexahydro-furo[3,4-b]furan-6-yloxy]-isoindole-1,3-dione(471241-75-5)

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: 471241-75-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 471241-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,1,2,4 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 471241-75:
(8*4)+(7*7)+(6*1)+(5*2)+(4*4)+(3*1)+(2*7)+(1*5)=135
135 % 10 = 5
So 471241-75-5 is a valid CAS Registry Number.

471241-75-5Upstream product

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471241-75-5Relevant academic research and scientific papers

Sequential alkoxy radical fragmentation-intermolecular allylation in carbohydrate systems

Martín, Angeles,Pérez-Martín, Inés,Suárez, Ernesto

, p. 4781 - 4784 (2002)

The C-radical originated by β-fragmentation of carbohydrate anomeric alkoxy radicals, generated under reductive conditions by treatment of N-phthalimido glycosides with allyltri-n-butyltin/AIBN, may subsequently undergo an intermolecular allylation to giv

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