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(4S,5R,6S)-4-[(E)-(S)-6-Hydroxy-10-(4-methoxy-phenyl)-4,8-dioxo-dec-1-enyl]-6-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-5-vinyl-5,6-dihydro-4H-pyran-3-carboxylic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • (4S,5R,6S)-4-[(E)-(S)-6-Hydroxy-10-(4-methoxy-phenyl)-4,8-dioxo-dec-1-enyl]-6-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-5-vinyl-5,6-dihydro-4H-pyran-3-carboxylic acid methyl ester

    Cas No: 161012-76-6

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  • Xi'an Lyna Bio-Tech Co., Ltd.
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  • (4S,5R,6S)-4-[(E)-(S)-6-Hydroxy-10-(4-methoxy-phenyl)-4,8-dioxo-dec-1-enyl]-6-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-5-vinyl-5,6-dihydro-4H-pyran-3-carboxylic acid methyl ester

    Cas No: 161012-76-6

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  • Wuhan Senwayer Century Chemical Co.,Ltd
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  • 161012-76-6 Structure
  • Basic information

    1. Product Name: (4S,5R,6S)-4-[(E)-(S)-6-Hydroxy-10-(4-methoxy-phenyl)-4,8-dioxo-dec-1-enyl]-6-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-5-vinyl-5,6-dihydro-4H-pyran-3-carboxylic acid methyl ester
    2. Synonyms:
    3. CAS NO:161012-76-6
    4. Molecular Formula:
    5. Molecular Weight: 634.678
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 161012-76-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (4S,5R,6S)-4-[(E)-(S)-6-Hydroxy-10-(4-methoxy-phenyl)-4,8-dioxo-dec-1-enyl]-6-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-5-vinyl-5,6-dihydro-4H-pyran-3-carboxylic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S,5R,6S)-4-[(E)-(S)-6-Hydroxy-10-(4-methoxy-phenyl)-4,8-dioxo-dec-1-enyl]-6-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-5-vinyl-5,6-dihydro-4H-pyran-3-carboxylic acid methyl ester(161012-76-6)
    11. EPA Substance Registry System: (4S,5R,6S)-4-[(E)-(S)-6-Hydroxy-10-(4-methoxy-phenyl)-4,8-dioxo-dec-1-enyl]-6-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-5-vinyl-5,6-dihydro-4H-pyran-3-carboxylic acid methyl ester(161012-76-6)
  • 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: 161012-76-6(Hazardous Substances Data)

161012-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161012-76-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,0,1 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 161012-76:
(8*1)+(7*6)+(6*1)+(5*0)+(4*1)+(3*2)+(2*7)+(1*6)=86
86 % 10 = 6
So 161012-76-6 is a valid CAS Registry Number.

161012-76-6Upstream product

161012-76-6Downstream Products

161012-76-6Relevant articles and documents

Absolute stereostructures of hydramacrosides A and B, new bioactive secoiridoid glucoside complexes from the leaves of Hydrangea macrophylla Seringe var thunbergii Makino

Yoshikawa,Ueda,Matsuda,Yamahara,Murakami

, p. 1691 - 1693 (1994)

Two new bioactive secoiridoid glucoside complexes named hydramacrosides A and B were isolated from the leaves of Hydrangea macrophylla Seringe var. thunbergii Makino. The absolute stereostructures of hydramacrosides A and B were elucidated on the basis of chemical and physicochemical evidence which included the application of the 13C NMR glycosylation shift rule of 1,1'-disaccharides and the modified Mosher's method. Hydramacrosides A and B exhibited inhibitory effect on the histamine release from rat mast cells induced by antigen-antibody reaction.

Chemical constituents from the leaves of Hydrangea macrophylla var. thunbergii (III): Absolute stereostructures of hydramacrosides A and B, secoiridoid glucoside complexes with inhibitory activity on histamine release

Matsuda, Hisashi,Shimoda, Hiroshi,Uemura, Toshiaki,Ueda, Tomohiko,Yamahara, Johji,Yoshikawa, Masayuki

, p. 1753 - 1758 (1999)

Following the characterization of dihydroisocoumarin constituents, two secoiridoid glucoside complexes, called hydramacrosides A and B, were isolated from the leaves of Hydrangea macrophylla SERINGE var. thunbergii MAKINO. The absolute stereostructures of hydramacrosides A and B were elucidated on the basis of chemical and physicochemical evidence, which included the application of the 13C-NMR glycosylation shift rule of 1,1'- disaccharides and the modified Mosher's method. Hydramacrosides A and B exhibited an inhibitory effect on histamine release from rat mast cells induced by an antigen-antibody reaction.

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