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1258-86-2

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  • 11H,13H-Oxireno[d]pyrano[4',3':3,3a]isobenzofuro[5,4-f][2]benzopyran-6,13(5aH)-dione,8-(3-furanyl)dodecahydro-4-hydroxy-2,2,4a,8a-tetramethyl-,(2aR,4S,4aS,4bR,5aS,8S,8aS,10aR,10bR,14aS)- (9CI) cas 12

    Cas No: 1258-86-2

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1258-86-2 Usage

Chemical class

Benzopyran derivative

Explanation

The compound belongs to the class of benzopyran derivatives, which are organic compounds containing a fused benzene and pyran ring.

Explanation

The compound has a furanyl group (a five-membered ring containing four carbon atoms and one oxygen atom) attached at the 8th position of the benzopyran core.

Explanation

The compound contains a hydroxyl (-OH) group at the 4th position, which can participate in hydrogen bonding and other interactions.

Explanation

The stereochemistry of the compound is specified by the given sequence of letters (R or S), which indicate the three-dimensional arrangement of the atoms in the molecule.

Explanation

The compound features oxireno (an oxirane ring with an additional oxygen atom) and pyrano (a six-membered oxygen-containing ring) heterocycles, which contribute to its unique chemical properties.

Explanation

The compound is a dodecahydro derivative, meaning it contains 12 hydrogen atoms in its fully saturated structure.

Explanation

The compound has four methyl (-CH3) groups attached at the 2, 2, 4a, and 8a positions, which can influence its steric properties and reactivity.

Explanation

The unique combination of oxygen-containing heterocycles and a furanyl group in the compound suggests that it may have interesting biological and chemical properties, making it a candidate for further research and potential applications.

Explanation

The IUPAC name provides a detailed description of the compound's structure, including the positions of various functional groups and stereochemistry.

Explanation

The 9CI identifier is a unique numerical code assigned to the compound by the Chemical Abstracts Service, which can be used to search for information about the compound in scientific databases.

Furanyl substituent

8-position

Hydroxyl group

4-hydroxy

Stereochemistry

2aR,4S,4aS,4bR,5aS,8S,8aS,10aR,10bR,14aS

Oxygen-containing heterocycles

Oxireno and pyrano

Dodecahydro

12 hydrogen atoms

Tetramethyl

2,2,4a,8a positions

Potential applications

Biological and chemical properties

Check Digit Verification of cas no

The CAS Registry Mumber 1258-86-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,5 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1258-86:
(6*1)+(5*2)+(4*5)+(3*8)+(2*8)+(1*6)=82
82 % 10 = 2
So 1258-86-2 is a valid CAS Registry Number.

1258-86-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Epilimonol

1.2 Other means of identification

Product number -
Other names epi-limonol

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:1258-86-2 SDS

1258-86-2Upstream product

1258-86-2Downstream Products

1258-86-2Relevant articles and documents

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 (2002)

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.

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