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4H-1-Benzopyran-4-one, 3-(2,4-dimethoxyphenyl)-2,3-dihydro-5,7-dimethoxy- is a complex organic compound belonging to the class of benzopyran derivatives. It is characterized by a benzopyran-4-one core structure, which features a benzene ring fused to a pyran ring, with a carbonyl group at the 4-position. The compound is further defined by the presence of a 2,4-dimethoxyphenyl group attached at the 3-position, which introduces two methoxy substituents on the phenyl ring. Additionally, the molecule has two methoxy groups at the 5 and 7 positions of the benzopyran ring. This specific arrangement of functional groups and substituents contributes to the compound's unique chemical properties and potential applications in various fields, such as pharmaceuticals or agrochemicals.

1100-14-7

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1100-14-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1100-14-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,0 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1100-14:
(6*1)+(5*1)+(4*0)+(3*0)+(2*1)+(1*4)=17
17 % 10 = 7
So 1100-14-7 is a valid CAS Registry Number.

1100-14-7Relevant academic research and scientific papers

Isoflavanones from the heartwood of Swartzia polyphylla and their antibacterial activity against cariogenic bacteria

Osawa,Yasuda,Maruyama,Morita,Takeya,Itokawa

, p. 2970 - 2974 (1992)

The methanolic extract of Swartzia polyphylla DC. heartwood had antibacterial activity against cariogenic bacteria, the mutans Streptococci. The chromatographic purification of the extract afforded seven flavonoids. Among them, three known isoflavanones, dihydrobiochanin A, ferreirin and darbergioidin, and one new isoflavanone, 5,2',4'-trihydroxy-7-methoxyisoflavanone (dihydrocajanin) had potent antibacterial activity against cariogenic bacteria. This effect was not detected on isoflavone derivatives. A comparative antibacterial study of various flavonoids was further performed, and their structure-activity relationship was discussed.

Organolead-mediated Arylation of Allyl β-Ketoesters: A Selective Synthesis of Isoflavanones and Isoflavones

Donnelly, Dervilla M.,Finet, Jean-Pierre,Rattigan, Bernard A.

, p. 1729 - 1736 (2007/10/02)

Arylation of A-ring substituted and unsabstituted 3-allyloxycarbonylchroman-4-ones with aryllead(IV) triacetates followed by selective catalytic deallyloxycarbonylation affords isoflavanones or isoflavones in high overall yields.The highest yield in the arylation step was observed in the reaction of 5,7-dimethoxychroman-4-one with the more hindered 2,4,6-trimethoxyphenyllead triacetate.

CATALYTIC TRANSFER HYDROGENATION, A CHEMO-SELECTIVE REDUCTION OF ISOFLAVONES TO ISOFLAVANONES

Krishnamurty, H.G.,Sathyanarayana, S.

, p. 1657 - 1664 (2007/10/02)

Isoflavones can be selectively reduced by catalytic transfer hydrogenation employing formic acid, ammonium formate or triethylammonium formate in the presence of 10percent Pd/C.The reaction is simple, clean and gives fair yields of isoflavanones.

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