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1983-72-8

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1983-72-8 Usage

General Description

MEDICAGOL is a chemical compound found in the leaves and stems of the Medicago plant, commonly known as alfalfa. It is classified as a phytoestrogen, which means it acts similarly to the hormone estrogen in the human body. MEDICAGOL has been studied for its potential health benefits, including its anti-inflammatory and anti-oxidant properties. It has also been investigated for its potential use in the treatment of menopausal symptoms and osteoporosis. Additionally, MEDICAGOL has been shown to have anti-cancer properties, particularly in the inhibition of cancer cell growth and proliferation. Further research is needed to fully understand the potential therapeutic applications of MEDICAGOL.

Check Digit Verification of cas no

The CAS Registry Mumber 1983-72-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,8 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1983-72:
(6*1)+(5*9)+(4*8)+(3*3)+(2*7)+(1*2)=108
108 % 10 = 8
So 1983-72-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H8O6/c17-7-1-2-8-10(3-7)22-16(18)14-9-4-12-13(20-6-19-12)5-11(9)21-15(8)14/h1-5,17H,6H2

1983-72-8Downstream Products

1983-72-8Relevant articles and documents

Jurd

, p. 1221,1222 (1965)

O-heterocycles via laccase-catalyzed domino reactions with O2 as the oxidant

Leutbecher, Heiko,Conrad, Jürgen,Klaiber, Iris,Beifuss, Uwe

, p. 3126 - 3130 (2007/10/03)

Laccase-catalyzed domino reactions of 4-hydroxy-6-methyl-2H-pyran-2-one or substituted 4-hydroxy-2H-chromen-2-ones with catechols using molecular oxygen as an oxidant afford coumestans and related O-heterocycles with yields ranging from 51% to 99%. Georg Thieme Verlag Stuttgart.

The first direct transformation of 2,2'-dihydroxychalcones into coumestans

Kamara, B. Irene,Brandt, E. Vincent,Ferreira, Daneel

, p. 861 - 868 (2007/10/03)

Three coumestans, flemichapparin, medicagol and sophoracoumestan B, are synthesised by direct reaction of the analogous 2,2'-dihydroxychalcones with thallium (III) nitrate in methanol.

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