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CAS

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17811-32-4

3-Deoxyzinnolide is a bioactive chemical compound naturally derived from Streptomyces bacteria, belonging to the butenolide class of compounds. It is recognized for its antimicrobial and antifungal properties, making it a promising candidate for pharmaceutical applications, particularly in the development of new antibiotics. Its unique structure and properties have garnered interest in the fields of drug discovery and biotechnology, with additional potential as an anti-inflammatory agent for the treatment of various diseases and medical conditions.

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  • 17811-32-4 Structure

  • Basic information

    1. Product Name: 3-Deoxyzinnolide
    2. Synonyms: 3-Deoxyzinnolide;6-[(3',3'-Dimethylallyl)oxy]-4-methoxy-5-methylphthalide
    3. CAS NO:17811-32-4
    4. Molecular Formula: C15H18O4
    5. Molecular Weight: 262.30102
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17811-32-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 448.6°Cat760mmHg
    3. Flash Point: 200.7°C
    4. Appearance: /
    5. Density: 1.141g/cm3
    6. Vapor Pressure: 3.05E-08mmHg at 25°C
    7. Refractive Index: 1.54
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-Deoxyzinnolide(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-Deoxyzinnolide(17811-32-4)
    12. EPA Substance Registry System: 3-Deoxyzinnolide(17811-32-4)

  • 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: 17811-32-4(Hazardous Substances Data)

17811-32-4 Usage

Uses

Used in Pharmaceutical Industry:
3-Deoxyzinnolide is used as a potential antibiotic for its antimicrobial properties, offering a new avenue for combating resistant bacteria and contributing to the development of novel therapeutic agents.
Used in Biotechnology Industry:
3-Deoxyzinnolide is utilized in research and development for its bioactive properties, with applications in drug discovery to create innovative treatments and therapies.
Used in Anti-inflammatory Applications:
3-Deoxyzinnolide is employed as a potential anti-inflammatory agent, targeting various diseases and medical conditions where inflammation plays a significant role, thereby expanding its therapeutic potential beyond just antimicrobial uses.

Check Digit Verification of cas no

The CAS Registry Mumber 17811-32-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,1 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17811-32:
(7*1)+(6*7)+(5*8)+(4*1)+(3*1)+(2*3)+(1*2)=104
104 % 10 = 4
So 17811-32-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H18O4/c1-9(2)5-6-18-13-7-11-12(8-19-15(11)16)14(17-4)10(13)3/h5,7H,6,8H2,1-4H3

17811-32-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxy-5-methyl-6-(3-methylbut-2-enoxy)-3H-2-benzofuran-1-one

1.2 Other means of identification

Product number -
Other names 5-<3,3-Dimethyl-allyloxy>-4-methoxy-5-methyl-phthalid

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:17811-32-4 SDS

17811-32-4Relevant articles and documents

Incorporation of carbon dioxide into phthalides: Via ligand-free copper-catalyzed direct carboxylation of benzoxasiloles

Nguyen, Thanh V. Q.,Rodríguez-Santamaría, José A.,Yoo, Woo-Jin,Kobayashi, Shu

, p. 2501 - 2505 (2017/07/17)

The direct carboxylation of benzoxasiloles with carbon dioxide proceeded smoothly under mild conditions using copper iodide as a catalyst to afford phthalides after an acid work-up. Broad substrate scope and application of this methodology for the synthesis of natural products highlight the synthetic utility of this protocol.

Natural zinniol derivatives from Alternaria tagetica. Isolation, synthesis, and structure-activity correlation.

Gamboa-Angulo, M Marcela,Escalante-Erosa, Fabiola,Garcia-Sosa, Karlina,Alejos-Gonzalez, Fatima,Delgado-Lamas, Guillermo,Pena-Rodriguez, Luis M

, p. 1053 - 1058 (2007/10/03)

Two novel phytotoxins, 8-zinniol methyl ether (5) and 8-zinniol acetate (6), in addition to 6-(3',3'-dimethylallyloxy)-4-methoxy-5-methylphthalide (2), 5-(3',3'-dimethylallyloxy)-7-methoxy-6-methylphthalide (3), and the novel metabolites 8-zinniol 2-(phenyl)ethyl ether (4) and 7-zinniol acetate (7) have been identified as natural zinniol derivatives from the organic crude extract of Alternaria tagetica culture filtrates. Using zinniol as the starting material, phytotoxin 5 was synthesized, together with a number of synthetic intermediates (8-13). Both natural and synthetic zinniol derivatives were evaluated in the leaf-spot bioassay against marigold leaves (Tagetes erecta).

Synthesis based on cyclohexadienes: Part 261 - Total synthesis of some naturally occurring phthalides from Alternaria species

Hariprakasha,Subba Rao

, p. 851 - 856 (2007/10/03)

Total synthesis of the naturally occurring phytotoxic phthalides, silvaticol 7, zinniol 5 and the phthalides 1 and 2, is reported from the substrate 16 derived from the Alder-Rickert reaction of 1-methoxy-2-methyl-3-trimethylsilyloxycyclohexa-1,3-diene 15

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