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pinocembrin 7-O-β-neohesperidoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30902-90-0

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30902-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30902-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,9,0 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30902-90:
(7*3)+(6*0)+(5*9)+(4*0)+(3*2)+(2*9)+(1*0)=90
90 % 10 = 0
So 30902-90-0 is a valid CAS Registry Number.

30902-90-0Downstream Products

30902-90-0Relevant academic research and scientific papers

TWO ACYLATED FLAVANONE GLYCOSIDES FROM NIEREMBERGIA HIPPOMANICA

Gonzalez, Maria D.,Pomilio, Alicia B.

, p. 757 - 760 (1982)

Two new acylated flavanone glycosides have been isolated from Nierembergia hippomanica and identified by spectral data as pinocembrin 7-O-β-(3"'-O-acetyl)neohesperidoside and pinocembrin 7-O-β-(6"-O-acetyl)neohesperidoside.Key Word Index - Nierembergia hippomanica; Solanaceae; acylated flavanone glycosides; pinocembrin 7-O-(3"'-O-acetyl)neohesperidoside; pinocembrin 7-O-β-(6"-O-acetyl)neohesperidoside.

STRUCTURAL ASPECTS OF ANTHOCYANIN-FLAVONOID COMPLEX FORMATION AND ITS ROLE IN PLANT COLOR

Chen, Lao-Jer,Hrazdina, Geza

, p. 297 - 304 (2007/10/02)

Key Word Index - Anthocyanin; flavonoid glycosides; synthesis; complex formation; plant color; spectral properties. The complex formation of flavonoids with anthocyanins, resulting in increase in both absorbance and in a bathochromic shift of the visible absorption maximum of the latter, is based mainly on hydrogen bond formation between the carbonyl group of the anthocyanin anhydrobase and aromatic hydroxyl groups of the complex-forming flavonoids.The larger the number of hydroxyl groups in the flavonoid molecule, the strongr the complex formation.The presence of a 3-hydroxyl group in the flavonoid molecule has little effect on the complex-forming ability.The nature of the sugar substituent of the complex-forming flavonoid compound has no influence on the reaction.The 5-hydroxyl group of flavonoids is strongly bound by intramolecular hydrogen bond to the 4-carbonyl and does not participate in the complex formation.The most important hydroxyl group in the flavonoid molecule is one in the 7-position.Unsaturation at C2-C3 in the heterocyclic ring is an important factor for complex formation.Aromatic hydroxyl groups in the flavonoid system alone cannot account for all the complex-forming ability, suggesting additional involvment by electrostatic forces and configurational or steric effects.

AN ACYLATED FLAVONOID FROM NIEREMBERGIA HIPPOMANICA

Gonzalez, M. D.,Pomilio, A. B.,Gros, E. G.

, p. 1174 - 1175 (2007/10/02)

A new acylflavonoid has been isolated from Nierembergia hippomanica and identified by chemical and spectral data as pinocembrin 7-O-β-(2"-O-acetyl)neohesperidoside.Key Word Index- Nierembergia hippomanica; Solanaceae; acylflavonoid; pinocembrin 7-O-β-(2"-O-acetyl)neohesperidoside.

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