Cas 593245-57-9,(2R,3R)-[5-methoxy-2-(4-methoxyphenyl)-2,3-dihydrobenzofuran-3-yl]methanol

593245-57-9

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Basic information

Product Name: (2R,3R)-[5-methoxy-2-(4-methoxyphenyl)-2,3-dihydrobenzofuran-3-yl]methanol
Synonyms:
CAS NO:593245-57-9
Molecular Formula:
Molecular Weight: 286.328
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: (2R,3R)-[5-methoxy-2-(4-methoxyphenyl)-2,3-dihydrobenzofuran-3-yl]methanol(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R)-[5-methoxy-2-(4-methoxyphenyl)-2,3-dihydrobenzofuran-3-yl]methanol(593245-57-9)
EPA Substance Registry System: (2R,3R)-[5-methoxy-2-(4-methoxyphenyl)-2,3-dihydrobenzofuran-3-yl]methanol(593245-57-9)

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: 593245-57-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 593245-57-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,3,2,4 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 593245-57:
(8*5)+(7*9)+(6*3)+(5*2)+(4*4)+(3*5)+(2*5)+(1*7)=179
179 % 10 = 9
So 593245-57-9 is a valid CAS Registry Number.

593245-57-9Upstream product

108-05-4 vinyl acetate

593245-57-9Downstream Products

593245-57-9Relevant academic research and scientific papers

Synthesis of optically active 2,3-dihydrobenzofuran derivatives through a combination strategy of iron(III)-catalyzed reaction and enzymatic reaction

Itoh, Toshiyuki,Kawai, Kimio,Hayase, Shuichi,Ohara, Hiroyuki

, p. 4081 - 4084 (2003)

Synthesis of optically active 2,3-dihydrofuran derivatives has been accomplished through a combination strategy of ferric ion-catalyzed cycloaddition of styrene derivatives with quinones and following lipase-catalyzed enantioselective acylation.

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