Cas 6200-02-8,(3-methoxy-5-oxo-4-phenyl-5<i>H</i>-furan-2-ylidene)-(2-methoxy-phenyl)-acetic acid methyl ester

6200-02-8

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Basic information

Product Name: (3-methoxy-5-oxo-4-phenyl-5H-furan-2-ylidene)-(2-methoxy-phenyl)-acetic acid methyl ester
Synonyms: (3-methoxy-5-oxo-4-phenyl-5H-furan-2-ylidene)-(2-methoxy-phenyl)-acetic acid methyl ester
CAS NO:6200-02-8
Molecular Formula:
Molecular Weight: 366.37
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: (3-methoxy-5-oxo-4-phenyl-5H-furan-2-ylidene)-(2-methoxy-phenyl)-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3-methoxy-5-oxo-4-phenyl-5H-furan-2-ylidene)-(2-methoxy-phenyl)-acetic acid methyl ester(6200-02-8)
EPA Substance Registry System: (3-methoxy-5-oxo-4-phenyl-5H-furan-2-ylidene)-(2-methoxy-phenyl)-acetic acid methyl ester(6200-02-8)

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: 6200-02-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 6200-02-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,0 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6200-02:
(6*6)+(5*2)+(4*0)+(3*0)+(2*0)+(1*2)=48
48 % 10 = 8
So 6200-02-8 is a valid CAS Registry Number.

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6200-02-8Downstream Products

6200-02-8Relevant academic research and scientific papers

Synthesis of leprapinic acid, calycine and analogues by sequential "[3+2] cyclization/suzuki/lactonization" reactions

Ahmed, Zafar,Albrecht, Uwe,Langer, Peter

, p. 3469 - 3474 (2007/10/03)

Calycine and analogues were prepared on the basis of Suzuki cross-coupling reactions of γ-alkylidene-α-hydroxybutenolides - readily available by cyclization of 1,3-dicarbonyl dianions or 1,3-bis(silyl enol ether)s with oxalyl derivatives - and subsequent boron tribromide-mediated lactonization. Leprapinic acid was prepared by chemoselective boron tribromide-mediated deprotection of permethylated leprapinic acid. Wiley-VCH Verlag GmbH & Co. KGaA, 2005.

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