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4,7,9-trihydroxy-1-(4-hydroxyphenyl)-6H-anthra[1,9-bc]furan-6-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1190948-58-3

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1190948-58-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1190948-58-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,9,4 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1190948-58:
(9*1)+(8*1)+(7*9)+(6*0)+(5*9)+(4*4)+(3*8)+(2*5)+(1*8)=183
183 % 10 = 3
So 1190948-58-3 is a valid CAS Registry Number.

1190948-58-3Downstream Products

1190948-58-3Relevant academic research and scientific papers

Convergent synthesis of diptoindonesin G

Singh, Dileep Kumar,Kim, Ikyon

, p. 300 - 301 (2019/01/04)

A convergent and scalable synthetic route to a tetracyclic oligostilbenoid natural product, diptoindonesin G, is described where Suzuki-Miyaura cross-coupling and intramolecular Friedel-Crafts acylation were employed to construct the central C ring of dip

Skeletal Reorganization: Synthesis of Diptoindonesin G from Pauciflorol F

Singh, Dileep Kumar,Kim, Ikyon

, p. 1667 - 1672 (2018/02/10)

Described herein is a novel synthetic approach to diptoindonesin G, a highly potent anticancer oligostilbenoid natural product, from pauciflorol F pentamethyl ether through a skeletal reorganization strategy where oxidative cleavage of the indanone ring system of pauciflorol F and sequential cyclization of the key intermediate allowed direct access to the target skeleton.

SYNTHESIS OF NOVEL ANALOGS OF DIPTOINDONESIN G, COMPOUNDS FORMED THEREBY, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

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Paragraph 0036; 0041, (2018/03/25)

Disclosed are unnatural analogs of Diptoindonesin G, methods to make the analogs, pharmaceutical compositions containing the analogs, and methods of using the analogs to inhibit neoplastic cell growth.

Total synthesis of diptoindonesin G and its analogues as selective modulators of estrogen receptors

Liu, Ji-Tian,Do, Truman J.,Simmons, Christopher J.,Lynch, John C.,Gu, Wen,Ma, Zhi-Xiong,Xu, Wei,Tang, Weiping

supporting information, p. 8927 - 8930 (2016/10/07)

We have developed a versatile synthetic strategy for the synthesis of the natural product diptoindonesin G and its analogues as selective modulators of estrogen receptors. The strategy involves a regioselective dehydrative cyclization of arylacetals, a regioselective bromination of benzofurans, a sequential cross-coupling of bromo-benzofurans with aryl boronic acids, and a BBr3-mediated tandem cyclization and demethylation. Preliminary biological studies uncovered the critical and dispensable phenolic hydroxyl groups in the natural product and also revealed unexpected selectivity for isoforms of estrogen receptor.

Total synthesis of diptoindonesin G via a highly efficient domino cyclodehydration/intramolecular friedel-crafts acylation/regioselective demethylation sequence

Kim, Kyungsun,Kim, Ikyon

supporting information; experimental part, p. 5314 - 5317 (2010/12/29)

A highly efficient total synthesis of diptoindonesin G is described employing a domino dehydrative cyclization/intramolecular Friedel-Crafts acylation/regioselective demethylation reaction of aryloxyketone 7 by the action of BCl3 wherein the tetracyclic 6H-anthra[1,9-bc]furan-6-one skeleton was constructed via the 3-arylbenzofuran in a one-pot manner. This is the first example of the strategic combination of these three reactions in a cascade fashion. The routes presented here allow for direct access to diptoindonesin G and its analogues.

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