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3,4-dihydroxy-β-phenethyl-O-α-L-rhamnopyranosyl-(1<*>3)-β-D-glucopyranoside dimethyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 90985-64-1 Structure
  • Basic information

    1. Product Name: 3,4-dihydroxy-β-phenethyl-O-α-L-rhamnopyranosyl-(1<*>3)-β-D-glucopyranoside dimethyl ether
    2. Synonyms:
    3. CAS NO:90985-64-1
    4. Molecular Formula:
    5. Molecular Weight: 490.505
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 90985-64-1.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: 3,4-dihydroxy-β-phenethyl-O-α-L-rhamnopyranosyl-(1<*>3)-β-D-glucopyranoside dimethyl ether(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4-dihydroxy-β-phenethyl-O-α-L-rhamnopyranosyl-(1<*>3)-β-D-glucopyranoside dimethyl ether(90985-64-1)
    11. EPA Substance Registry System: 3,4-dihydroxy-β-phenethyl-O-α-L-rhamnopyranosyl-(1<*>3)-β-D-glucopyranoside dimethyl ether(90985-64-1)
  • 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: 90985-64-1(Hazardous Substances Data)

90985-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90985-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,9,8 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90985-64:
(7*9)+(6*0)+(5*9)+(4*8)+(3*5)+(2*6)+(1*4)=171
171 % 10 = 1
So 90985-64-1 is a valid CAS Registry Number.

90985-64-1Relevant articles and documents

A new glycoside, brachynoside, isolated from Clerodendron brachyanthum Schauer

Lin,Kuo

, p. 1928 - 1929 (2007/10/02)

Eudesmin, syringaresinol dimethyl ether, kusaginin and brachynoside were isolated from the ethanol extract of the leaves of Clerodendron brachyanthum. The new glycoside, branchynoside, was assigned as 2-(3,4-dimethoxyphenyl)ethyl 3-O-α-L-rhamnopyranosyl-4-O-(3,4-dihydroxycinnamoyl)-β-D-glucopyrano side from studies on partial methylation and methanolysis products and from analysis of spectroscopic evidence.

160. Lavandulifolioside: A New Phenylpropanoid Glycoside from Stachys lavandulifolia

Basaran, Arif Ahmet,Calis, Ihsan,Anklin, Clemens,Nishibe, Sansei,Sticher, Otto

, p. 1483 - 1490 (2007/10/02)

A new phenylpropanoid glycoside has been isolated from the methanolic extract of the aerial parts of Stachys lavandulifolia (Lamiaceae), lavandulifolioside (1).On the basis of chemical and spectral data the structure of the new compound 1 has been elucidated as β-(3,4-dihydroxyphenyl)ethyl O-α-L-arabinopyranosyl-(1->2)-α-L-rhamnopyranosyl-(1->3)-4-O-caffeoyl-β-D-glucopyranoside.

PHENYLPROPANOID GLYCOSIDES ISOLATED FROM SCROPHULARIA SCOPOLI

Calis, Ihsan,Gross, Gian-Andrea,Sticher, Otto

, p. 2057 - 2062 (2007/10/02)

Key Word Index - Scrophularia scopolii var. scopolii; Scrophulariaceae; phenylpropanoid glycosides; acteoside; verbascoside; angoroside A; deacyl angoroside A dimethyl ether; deacyl acteoside dimethyl ether. A new phenylpropanoid glycoside, angoroside A, and a known glycoside, acteoside, were isolated from the roots of Scrophularia scopolii var. scopolii.On the basis of chemical and spectral evidence, angoroside A was shown to be 3,4-dihydroxy-β-phenylethoxy-O-α-L-arabinopyranosyl-(1->6)-α-L-rhamnopyranosyl-(1->3)-4-O-caffeoyl-β-D-glucopyranoside.

IRIDOID AND PHENOLIC GLYCOSIDES FROM HARPAGOPHYTUM PROCUMBENS

Burger, Johann F. W.,Brandt, E. Vincent,Ferreira, Daneel

, p. 1453 - 1458 (2007/10/02)

Key Word Index - Harpagophytum procumbens; Pedaliaceae; iridoid and phenolic glycosides; synthesis.A novel bioside, β-(3',4'-dihydroxyphenyl)ethyl-O-α-L-rhamnopyranosyl(1 -> 3)-β-D-glucopyranoside, was obtained from the secondary roots of Harpagophytum procumbens.It is accompained by the known iridoid glucosides harpagoside, procumbide, and its 6'-O-p-coumaroyl ester, and phenolic glycosides, acteoside and isoacteoside, the latter pair being obtained from H. procumbens for the first time.The structures of these metabolites were differentiated by high resolution NMR studies, while that of the bioside is additionally supported by synthesis.

BITTER PHENYL PROPANOID GLYCOSIDES FROM CAMPSIS CHINENSIS

Imakura, Yasuhiro,Kobayashi, Shigeru,Mima, Akira

, p. 139 - 146 (2007/10/02)

Key Word Index - Campsis chinensis; Bignoniaceae; bitter phenyl propanoid glycosides; R,S-β-methoxy-β-(3',4'-dihydroxyphenyl)-ethyl alcohol; R,S-β-hydroxy-β-(3',4'-dihydroxyphenyl)-ethyl alcohol; caffeic acid; acteoside; campneoside I; campneoside II.A new bitter phenyl propanoid glycoside, campneoside I, was isolated, together with acteoside and campneoside II, from the leaves of Campsis chinensis.The stereostructure of campneoside I was established as R,S-β-methoxy-β-(3',4'-dihydroxyphenyl)-ethyl-O-α-L-rhamnopyranosyl(1->3)-β-D-(4-O-caffeoyl)-glucopyranoside on the basis of the spectroscopic studies and chemical evidence.

Studies on the Chinese Crude Drug "Forsythiae Fructus." VII. A New Caffeoyl Glycoside from Forsythia viridissima

Kitagawa, Shizuka,Tsukamoto, Hiroki,Hisada, Sueo,Nishibe, Sansei

, p. 1209 - 1213 (2007/10/02)

In addition to a known caffeoyl glycoside of 3,4-dihydroxyphenethyl alcohol, acteoside (1), a new caffeoyl glycoside of β,3,4-trihydroxyphenethyl alcohol, designated as β-hydroxyacteoside (2), was isolated from the fruits of Forsythia viridissima LINDLEY (Oleaceae).The structure of 2 was established as β,3,4-trihydroxyphenethyl-O-α-L-rhamnopyranosyl-(1->3)-4-O-caffeoyl-β-D-glucopyranoside on the basis of analysis of the carbon-13 nuclear magnetic resonance spectrum and chemical evidence.Keywords - Forsythia viridissima; Oleaceae; acteoside; caffeoyl glycoside of β,3,4-trihydroxyphenethyl alcohol; β-hydroxyacteoside; 13C-NMR spect ra

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