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2H-1-Benzopyran-3,4,7-triol, 2-(3,4-dihydroxyphenyl)-3,4-dihydro, (2S,3R,4R)- is a complex organic compound with the molecular formula C15H12O7. 2H-1-Benzopyran-3,4,7-triol, 2-(3,4-dihydroxyphenyl)-3,4-dihydro-, (2S,3R,4R)- is a stereoisomer, specifically the (2S,3R,4R)-enantiomer, which means it has a unique three-dimensional arrangement of atoms. It is derived from the benzopyran class of compounds, which are heterocyclic organic compounds containing a benzene ring fused to a pyran ring. The presence of multiple hydroxyl groups (-OH) at positions 3, 4, and 7, as well as the dihydroxyphenyl group at position 2, suggests that 2H-1-Benzopyran-3,4,7-triol, 2-(3,4-dihydroxyphenyl)-3,4-dihydro-, (2S,3R,4R)- may have potential applications in the pharmaceutical or chemical industries, possibly as a precursor to other compounds or as a functional group in its own right.

490-32-4

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490-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 490-32-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 490-32:
(5*4)+(4*9)+(3*0)+(2*3)+(1*2)=64
64 % 10 = 4
So 490-32-4 is a valid CAS Registry Number.

490-32-4Upstream product

490-32-4Downstream Products

490-32-4Relevant academic research and scientific papers

Oligomeric flavanoids. Part 26. Structure and synthesis of the first profisetinidins with epifisetinidol constituent units

Steynberg, Petrus J.,Steynberg, Jan P.,Brandt, E. Vincent,Ferreira, Daneel,Hemingway, Richard W.

, p. 1943 - 1950 (2007/10/03)

The natural occurrence of the first oligomeric profisetinidins with (2R,3R)-2,3-cis-epifisetinidol chain extender units is demonstrated in the bark of Pithecellobium dulce (Guamuchil). Semi-synthesis using the appropriate flavan-3-ol and flavan-3,4-diol precursors permits unequivocal structural and stereochemical assignment of the novel dimeric epifisetinidol-(4β,8)-catechin and epicatechins 16 and 18, the trimeric bis-epifisetinidol-(4β,6:4β,8)-catechin and epicatechins 33 and 35, the fisetinidol-(4α,8)-catechin-(6,4β)-epifisetinidol 37 and fisetinidol-(4α,8)-epicatechin-(6,4β)-epifisetinidol 39.

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