Cas 83307-79-3,(E)-2-(4-Chloro-phenyl)-3-(5-methyl-furan-2-yl)-acrylic acid

83307-79-3

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Basic information

Product Name: (E)-2-(4-Chloro-phenyl)-3-(5-methyl-furan-2-yl)-acrylic acid
Synonyms: (E)-2-(4-Chloro-phenyl)-3-(5-methyl-furan-2-yl)-acrylic acid
CAS NO:83307-79-3
Molecular Formula:
Molecular Weight: 262.693
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: (E)-2-(4-Chloro-phenyl)-3-(5-methyl-furan-2-yl)-acrylic acid(CAS DataBase Reference)
NIST Chemistry Reference: (E)-2-(4-Chloro-phenyl)-3-(5-methyl-furan-2-yl)-acrylic acid(83307-79-3)
EPA Substance Registry System: (E)-2-(4-Chloro-phenyl)-3-(5-methyl-furan-2-yl)-acrylic acid(83307-79-3)

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: 83307-79-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 83307-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,0 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83307-79:
(7*8)+(6*3)+(5*3)+(4*0)+(3*7)+(2*7)+(1*9)=133
133 % 10 = 3
So 83307-79-3 is a valid CAS Registry Number.

83307-79-3Upstream product

83307-79-3Downstream Products

83307-96-4 7a-hydroxy-2-methyl-6-(4-chlorophenyl)-3a,7a-dihydrofuro<3,2-b>pyran-5-one

83307-79-3Relevant academic research and scientific papers

PHOTOCHEMISTRY OF FURANS. PHOTOCHEMICAL TRANSFORMATIONS OF SOME SUBSTITUTED 2-PHENYL-3-FURYLACRYLIC ACIDS

Karminski-Zamola, G.,Fiser-Jakic, L.,Jakopcic, K.

, p. 1329 - 1335 (2007/10/02)

A number of new substituted 2-phenyl-3-furylacrylic acids (1-14) were synthesized by modified Perkin reaction and separated into their E- and Z-isomers and identified by spectroscopic methods.E-isomers were UV-irradiated under aerobic conditions to give s

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