Cas 869486-19-1,4-hydroxy-4-(3-hydroxymethyl-benzofuran-2-yl)-3-methoxy-cyclohexa-2,5-dienone

869486-19-1

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Basic information

Product Name: 4-hydroxy-4-(3-hydroxymethyl-benzofuran-2-yl)-3-methoxy-cyclohexa-2,5-dienone
Synonyms: 4-hydroxy-4-(3-hydroxymethyl-benzofuran-2-yl)-3-methoxy-cyclohexa-2,5-dienone
CAS NO:869486-19-1
Molecular Formula:
Molecular Weight: 286.284
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: 4-hydroxy-4-(3-hydroxymethyl-benzofuran-2-yl)-3-methoxy-cyclohexa-2,5-dienone(CAS DataBase Reference)
NIST Chemistry Reference: 4-hydroxy-4-(3-hydroxymethyl-benzofuran-2-yl)-3-methoxy-cyclohexa-2,5-dienone(869486-19-1)
EPA Substance Registry System: 4-hydroxy-4-(3-hydroxymethyl-benzofuran-2-yl)-3-methoxy-cyclohexa-2,5-dienone(869486-19-1)

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: 869486-19-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 869486-19-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,4,8 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 869486-19:
(8*8)+(7*6)+(6*9)+(5*4)+(4*8)+(3*6)+(2*1)+(1*9)=241
241 % 10 = 1
So 869486-19-1 is a valid CAS Registry Number.

869486-19-1Upstream product

95338-37-7 2-methoxy-p-benzoquinone dimethyl acetal

869486-19-1Downstream Products

869486-19-1Relevant academic research and scientific papers

Phytochemical medicinal agents. a quinone-based route to pterocarpins

Kraus, George A.,Wei, Jingqiang

, p. 7511 - 7513 (2005)

The synthesis of 6,9 di-demethoxy kushecarpin A has been achieved by the coupling of a benzofuran anion with a quinone monoketal followed by a regioselective cyclization and a stereoselective hydrogenation reaction.

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