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7α-Obakunol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 17182-59-1 Structure
  • Basic information

    1. Product Name: 7α-Obakunol
    2. Synonyms: 7-Deoxo-7α-hydroxyobacunoic acid ε-lactone;7α-Obacunol;7α-Obakunol
    3. CAS NO:17182-59-1
    4. Molecular Formula: C26H32O7
    5. Molecular Weight: 456.52808
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17182-59-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 7α-Obakunol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7α-Obakunol(17182-59-1)
    11. EPA Substance Registry System: 7α-Obakunol(17182-59-1)
  • 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: 17182-59-1(Hazardous Substances Data)

17182-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17182-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,8 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17182-59:
(7*1)+(6*7)+(5*1)+(4*8)+(3*2)+(2*5)+(1*9)=111
111 % 10 = 1
So 17182-59-1 is a valid CAS Registry Number.

17182-59-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 7α-obacunol

1.2 Other means of identification

Product number -
Other names α-Obacunol

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:17182-59-1 SDS

17182-59-1Downstream Products

17182-59-1Relevant articles and documents

Insight into reduction of obacunone, and their ester derivatives as insecticidal agents against Mythimna separata Walker

Yu, Xiang,Ding, Guodong,Zhi, Xiaoyan,Xu, Hui

supporting information, p. 25 - 29 (2015/02/19)

Here we have prepared a series of ester compounds of obacunone, a naturally occurring limonoid, isolated from plants such as Citrus and Dictamnus angustifolius. Their insecticidal activity was evaluated at 1 mg/mL against the pre-third-instar larvae of or

Citrus limonoids and their semisynthetic derivatives as antifeedant agents against Spodoptera frugiperda larvae. A structure-activity relationship study

Ruberto, Giuseppe,Renda, Agatino,Tringali, Corrado,Napoli, Edoardo M.,Simmonds, Monique S. J.

, p. 6766 - 6774 (2007/10/03)

The antifeedant activity of Citrus-derived limonoids limonin (1), nomilin (2), and obacunone (3) and their semisynthetic derivatives 4-26 was evaluated against a commercially important pest, Spodoptera frugiperda. Simple chemical conversions were carried out on the natural limonoids obtained from seeds of Citrus limon. These conversions focused on functional groups considered to be important for the biological activity, namely the C-7 carbonyl and the furan ring. In particular, reduction at C-7 afforded the related alcohols, and from these their acetates, oximes, and methoximes were prepared. Hydrogenation of the furan ring was also performed on limonin and obacunone. The known antifeedant properties of the Citrus limonoids are confirmed. Comparison with previously reported data shows that insect species vary in their behavioral responses to these structural modifications. Highly significant antifeedant activity (P 0.01) for two natural (1 and 3) and three semisynthetic limonoids (4, 8, and 10) was observed against S. frugiperda.

Studies on the constituents of edible and medicinal plants. III. Effects of seven limonoids on the sleeping time induced in mice by anesthetics

Wada,Yagi,Kurihara,Haga

, p. 3079 - 3080 (2007/10/02)

Effects of seven limonoids, obakunone (1), 7α-obakunol (2), 7β-obakunol (3), limonin (4), 7α-limonol (5), 7β-limonol (6) and nomilin (7), on the sleeping time induced in mice by anesthetics were assayed. All the limonoids, except for 2, shortened the sleeping time induced by α-chloralose and urethane. 7 gave the highest reduction rate of sleeping time, and the order of the reduction rate of sleeping time was as follows; 7 > 1 and 3 > 4, 5 and 6. As the chemical structures of these compounds are similar to each other, the relationship between the structure and the effects of limonoids on sleeping time was discussed.

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