Cas 813430-48-7,2-Furancarboxylic acid, 4-[[(2E)-1,4-dioxo-3-(phenylmethyl)-2-pentenyl]oxy]-4,5-dihydro-5-meth oxy-, methyl ester, (4R,5R)-

813430-48-7

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Basic information

Product Name: 2-Furancarboxylic acid, 4-[[(2E)-1,4-dioxo-3-(phenylmethyl)-2-pentenyl]oxy]-4,5-dihydro-5-meth oxy-, methyl ester, (4R,5R)-
Synonyms:
CAS NO:813430-48-7
Molecular Formula: C19H20O7
Molecular Weight: 360.364
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-Furancarboxylic acid, 4-[[(2E)-1,4-dioxo-3-(phenylmethyl)-2-pentenyl]oxy]-4,5-dihydro-5-meth oxy-, methyl ester, (4R,5R)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Furancarboxylic acid, 4-[[(2E)-1,4-dioxo-3-(phenylmethyl)-2-pentenyl]oxy]-4,5-dihydro-5-meth oxy-, methyl ester, (4R,5R)-(813430-48-7)
EPA Substance Registry System: 2-Furancarboxylic acid, 4-[[(2E)-1,4-dioxo-3-(phenylmethyl)-2-pentenyl]oxy]-4,5-dihydro-5-meth oxy-, methyl ester, (4R,5R)-(813430-48-7)

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: 813430-48-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 813430-48-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,3,4,3 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 813430-48:
(8*8)+(7*1)+(6*3)+(5*4)+(4*3)+(3*0)+(2*4)+(1*8)=137
137 % 10 = 7
So 813430-48-7 is a valid CAS Registry Number.

813430-48-7Upstream product

2550-26-7 4-Phenyl-2-butanone

813430-48-7Downstream Products

813430-48-7Relevant academic research and scientific papers

Elaboration of D-(-)-ribose into a tricyclic, natural product-like scaffold

Messer, Roland,Schmitz, Andrea,Moesch, Luzia,Haener, Robert

, p. 8558 - 8560 (2004)

The construction of natural product-like, tricyclic compounds is reported. Starting from a D-(-)-ribose-derived dihydrofurane, the tricyclic scaffold is prepared via an intramolecular hetero-Diels-Alder reaction. The reaction proceeds with very high diast

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