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20108-30-9

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  • a-D-Glucopyranoside,(1S,4R,5R,6R,6aS,9S,10aR)-3-[(1S)-2-(acetyloxy)-1-methylethyl]-1,2,4,5,6,6a,7,8,9,10a-decahydro-1,5-dihydroxy-9-(methoxymethyl)-6,10a-dimethyldicyclopenta[a,d]cycloocten-4-yl6-O-(1

    Cas No: 20108-30-9

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  • a-D-Glucopyranoside,(1S,4R,5R,6R,6aS,9S,10aR)-3-[(1S)-2-(acetyloxy)-1-methylethyl]-1,2,4,5,6,6a,7,8,9,10a-decahydro-1,5-dihydroxy-9-(methoxymethyl)-6,10a-dimethyldicyclopenta[a,d]cycloocten-4-yl6-O-(1

    Cas No: 20108-30-9

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  • a-D-Glucopyranoside,(1S,4R,5R,6R,6aS,9S,10aR)-3-[(1S)-2-(acetyloxy)-1-methylethyl]-1,2,4,5,6,6a,7,8,9,10a-decahydro-1,5-dihydroxy-9-(methoxymethyl)-6,10a-dimethyldicyclopenta[a,d]cycloocten-4-yl6-O-(1

    Cas No: 20108-30-9

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  • 20108-30-9 Structure

  • Basic information

    1. Product Name: FUSICOCCIN
    2. Synonyms: FUSICOCCIN;fusicoccin from fusicoccum amygdali;3-[2-(Acetyloxy)-1-methylethyl]-1,2,4,5,6,6a,7,8,9,10a-decahydro-1,5-dihydroxy-9-(methoxymethyl)-6,10a-dimethylcyclopenta[a,d]-dicylo coten-4-yl-6;.alpha.-D-Glucopyranoside, 3-[2-(acetyloxy)-1-methylethyl]-1,2,4,5,6,6A,7,8,9,10A-decahydro-1,5-dihydroxy-9-(methoxymethyl)-6,10A-dimethyldicyclopenta[A,D]cycloocten-4-yl 6-o-(1,1-dimethyl-2-propenyl)-, 3-acetate, [1S-[1.alpha.,3(R*),4.alpha.,5.beta.,6.beta.,6A.alpha.,9.beta.,10A.beta.]]-;Fucicoccin;Fusicoccin a;Nsc113500
    3. CAS NO:20108-30-9
    4. Molecular Formula: C36H56O12
    5. Molecular Weight: 680.82
    6. EINECS: N/A
    7. Product Categories: Carbohydrates;Carbohydrates A to;Carbohydrates D-FBiochemicals and Reagents;Monosaccharide
    8. Mol File: 20108-30-9.mol
    9. Article Data: 1

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 760.2°Cat760mmHg
    3. Flash Point: 227°C
    4. Appearance: /
    5. Density: 1.24g/cm3
    6. Vapor Pressure: 1.12E-26mmHg at 25°C
    7. Refractive Index: 1.555
    8. Storage Temp.: −20°C
    9. Solubility: N/A
    10. CAS DataBase Reference: FUSICOCCIN(CAS DataBase Reference)
    11. NIST Chemistry Reference: FUSICOCCIN(20108-30-9)
    12. EPA Substance Registry System: FUSICOCCIN(20108-30-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 20108-30-9(Hazardous Substances Data)

20108-30-9 Usage

Uses

Fusicoccin is a 14-3-3-dependent activator of H+-ATPase.

Check Digit Verification of cas no

The CAS Registry Mumber 20108-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,0 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20108-30:
(7*2)+(6*0)+(5*1)+(4*0)+(3*8)+(2*3)+(1*0)=49
49 % 10 = 9
So 20108-30-9 is a valid CAS Registry Number.
InChI:InChI=1/C36H56O12/c1-10-35(6,7)45-17-26-30(41)33(46-21(5)38)31(42)34(47-26)48-32-28-24(18(2)15-44-20(4)37)13-27(39)36(28,8)14-25-22(16-43-9)11-12-23(25)19(3)29(32)40/h10,14,18-19,22-23,26-27,29-34,39-42H,1,11-13,15-17H2,2-9H3/b25-14-/t18-,19-,22-,23+,26-,27+,29-,30-,31-,32-,33+,34-,36+/m1/s1

20108-30-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name fusicoccin

1.2 Other means of identification

Product number -
Other names Fucicoccin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:20108-30-9 SDS

20108-30-9Downstream Products

20108-30-9Relevant articles and documents

Conversion of [19-2H2]fusicocca-2,10(14)-diene into its 8β-ol and fusicoccins by Phomopsis (Fusicoccum) amygdali

Sassa, Takeshi,Zhang, Chang-Shan,Sato, Mitsuyoshi,Tajima, Naoto,Kato, Nobuo,Mori, Akira

, p. 2401 - 2404 (2007/10/03)

Feeding experiments of (+)-[19-2H2]fusicocca-2,10(14)-diene, a deuterated derivative of a new candidate for the initially-forming fusicoccane-hydrocarbon in the fusicoccin biosynthesis, with the fusicoccin- producing fungus Phomopsis (Fusicoccum) amygdali have revealed its incorporation into fusicoccins J and A through (+)-fusicocca-2,10(14)-dien- 8β-ol, whose occurrence in the mycelial extract has been confirmed by direct comparison of its 1H NMR and GC-MS data with those of the synthetic sample, proving the early biosynthetic route leading to the aglycons of fusicoccins. (C) 2000 Elsevier Science Ltd.

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