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[(1R,3S,9S,11R)-3,11-Bis-carboxymethyl-7-(3,4-dimethoxy-benzoyl)-4,4,10,10-tetramethyl-8,13-dioxo-5-oxa-tricyclo[7.3.1.01,6]tridec-6-en-9-yl]-acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71103-16-7

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71103-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71103-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,1,0 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71103-16:
(7*7)+(6*1)+(5*1)+(4*0)+(3*3)+(2*1)+(1*6)=77
77 % 10 = 7
So 71103-16-7 is a valid CAS Registry Number.

71103-16-7Relevant academic research and scientific papers

Xanthochymol and Isoxanthochymol, Two Novel Polyisoprenylated Benzophenones from Gracinia xanthochymus

Rao, A. V. Rama,Ventkatswamy, G.,Yemul, S. S.

, p. 627 - 633 (2007/10/02)

Two optically active polyprenylated benzophenone derivates, (+)-xanthochymol and (+)-isoxanthochymol have been isolated from the fruits of Gracinia xanthochymus (fam.: Guttiferae).Both these compounds possess the same molecular formula, C38H50O6, and have many common features.Xanthochymol has a free enolic hydroxyl group which forms a part of the chroman ring in isoxanthochymol.Chemical and spectral evidence clearly indicate that both these compounds are derived from maclurin (2,4,6,3',5'-pentahydroxybenzophenone) in which the acetate derived phloroglucinol ringbecomes the target of attack by five "active isoprene" groups.Although, a partial structure has been suggested, the final structure for (+)-isoxanthochymol (V) has been established by X-ray analysis.Spectral evidence including 13C NMR data leads to structure (VIII) for (+)-xanthochymol which has also been arrived at independently by Blount and Williams . (+)-Xanthochymol has been smoothly converted to (+)-isoxanthochymol by acid-catalysed reactions.Bronianone isolated earlier by Ollis et al., from G. hambroniana has the same basic skeleton as xanthochymol and can be represented as X instead of having a bicyclooctene system.

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