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52210-15-8

(6R,7E,9R)-9-Hydroxy-4,7-megastigmadien-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52210-15-8 Structure

  • Basic information

    1. Product Name: (6R,7E,9R)-9-Hydroxy-4,7-megastigmadien-3-one
    2. Synonyms: (6R)-1,5,5-Trimethyl-6β-[(1E,3R)-3-hydroxy-1-butenyl]-1-cyclohexene-3-one;(6R,7E,9R)-9-Hydroxy-4,7-megastigmadien-3-one;(R)-4-[(R,E)-3-Hydroxy-1-butenyl]-3,5,5-trimethyl-2-cyclohexen-1-one
    3. CAS NO:52210-15-8
    4. Molecular Formula: C13H20O2
    5. Molecular Weight: 208.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52210-15-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 315.8±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.026±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 14.28±0.20(Predicted)
    10. CAS DataBase Reference: (6R,7E,9R)-9-Hydroxy-4,7-megastigmadien-3-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: (6R,7E,9R)-9-Hydroxy-4,7-megastigmadien-3-one(52210-15-8)
    12. EPA Substance Registry System: (6R,7E,9R)-9-Hydroxy-4,7-megastigmadien-3-one(52210-15-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 52210-15-8(Hazardous Substances Data)

52210-15-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52210-15-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,1 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52210-15:
(7*5)+(6*2)+(5*2)+(4*1)+(3*0)+(2*1)+(1*5)=68
68 % 10 = 8
So 52210-15-8 is a valid CAS Registry Number.

52210-15-8Relevant articles and documents

Enantiocontrolled access to the ionone type bisnorsesquiterpenes. Total syntheses of 3-oxo-α-ionol and related natural products

Kikuchi, Daisuke,Yoshida, Masahiro,Shishido, Kozo

, p. 145 - 147 (2012/01/17)

The enantiocontrolled total syntheses of three ionone type bisnorsesquiterpenes have been accomplished employing a highly diastereoselective intramolecular Heck reaction as the key step.

Megastigmane glycosides from seeds of Trifolium alexandrinum

Mohamed, Khaled M.,Mohamed, Mahmoud H.,Ohtani, Kazuhiro,Kasai, Ryoji,Yamasaki, Kazuo

, p. 859 - 862 (2007/10/03)

Five megastigmane glycosides have been isolated from the seeds of Trifolium alexandrinum L., of which two are known compounds, while three are new compounds showing the presence of apiofuranosyl-(1→2)-glucopyranosyl residue as a sugar moiety. The structures of the isolated compounds were established on the basis of NMR and mass spectral data.

TWO DIASTEREOMERIC 3-OXO-α-IONOL β-D-GLUCOSIDES FROM RASPBERRY FRUIT

Pabst, Anni,Barron, Denis,Semon, Etienne,Schreier, Peter

, p. 1649 - 1652 (2007/10/02)

From a methanolic extract of raspberry fruit two 3'-O-β-D-glucopyranosides of diastereomeric 4-(3'-hydroxy-1'-butenyl)-3,3,5-trimethyl-2-cyclohexen-1-one (3-oxo-α-ionol) were isolated by adsorption chromatography on XAD-2 followed by LC on Sephadex LH-20,

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