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489-53-2

7-Methoxy-8-(3,3-dimethylglycidyl)-2H-1-benzopyran-2-one is a complex organic compound with the molecular formula C16H16O4. It is a derivative of 2H-1-benzopyran-2-one, which is a type of chromone. This specific compound features a 7-methoxy group, which is a methoxy group attached to the 7th carbon, and an 8-(3,3-dimethylglycidyl) group, indicating a glycidyl moiety with two methyl groups attached to the 3rd carbon. The compound is characterized by its unique structure and potential applications in various fields, such as pharmaceuticals or chemical research. Due to its specific functional groups, it may exhibit unique chemical properties and reactivity, making it a subject of interest for scientists studying the synthesis and applications of complex organic molecules.

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  • 489-53-2 Structure

  • Basic information

    1. Product Name: 7-Methoxy-8-(3,3-dimethylglycidyl)-2H-1-benzopyran-2-one
    2. Synonyms: 7-Methoxy-8-(3,3-dimethylglycidyl)-2H-1-benzopyran-2-one;8-[(3,3-Dimethyloxiranyl)methyl]-7-methoxy-2H-1-benzopyran-2-one;Aurapten【C15H16O4】;Merangin
    3. CAS NO:489-53-2
    4. Molecular Formula: C15H16 O4
    5. Molecular Weight: 260.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 489-53-2.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: 7-Methoxy-8-(3,3-dimethylglycidyl)-2H-1-benzopyran-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-Methoxy-8-(3,3-dimethylglycidyl)-2H-1-benzopyran-2-one(489-53-2)
    11. EPA Substance Registry System: 7-Methoxy-8-(3,3-dimethylglycidyl)-2H-1-benzopyran-2-one(489-53-2)

  • 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: 489-53-2(Hazardous Substances Data)

489-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 489-53-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 489-53:
(5*4)+(4*8)+(3*9)+(2*5)+(1*3)=92
92 % 10 = 2
So 489-53-2 is a valid CAS Registry Number.

489-53-2SDS

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 8-[(3,3-Dimethyl-2-oxiranyl)methyl]-7-methoxy-2H-chromen-2-one

1.2 Other means of identification

Product number -
Other names methyl hydrogenpimelate

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:489-53-2 SDS

489-53-2Relevant articles and documents

Synthesis and biological evaluation of novel osthol derivatives as potent cytotoxic agents

Farooq, Saleem,Banday, Javid A.,Hussain, Aashiq,Nazir, Momina,Qurishi, Mushtaq A.,Hamid, Abid,Koula, Surrinder

, p. 138 - 149 (2019/06/11)

Background: Natural product, osthol has been found to have important biological and pharmacological roles particularly having inhibitory effect on multiple types of cancer. Objective: The unmet needs in cancer therapeutics make its derivatization an impor

TASTE MODIFYING COMPOUND

-

Page/Page column 10-11, (2013/02/28)

The present invention relates to the use of Formula (I) where Y represents * denoting the point at which the moiety bonds to the bicyclic ring, in any one of its stereoisomenc forms or mixtures thereof to confer, enhance, impart and/or modify the tingling sensation.

Identification and structure-activity relationship studies of osthol, a cytotoxic principle from Cnidium monnieri

Hitotsuyanagi, Yukio,Kojima, Hiroshi,Ikuta, Hiroshi,Takeya, Koichi,Itokawa, Hideji

, p. 1791 - 1794 (2007/10/03)

Osthol (1) was isolated from the fruit of Cnidium monnieri as a cytotoxic principle. Its structure-activity relationship study reveals that the 3,4-olefinic bond is essential for its cytotoxic activity, and the prenyl (C5) unit attached at the 8 position enhances the cytotoxicity. Analogues 7 and 8 that have a longer alkoxy unit at the 7 position showed ten times higher cytotoxicity than 1.

Side-chain bromination of osthol using N-bromosuccinimide and some related reactions

Krishnaswamy, N. R.,Vijayan, K. K.

, p. 664 - 666 (2007/10/02)

Osthol when treated with N-bromosuccinimide under free radical conditions gives 8-(3-bromomethyl-2-butenyl)-7-methoxycoumarin (2), whereas under ionic conditions the product obtained is 8-(2-bromo-3-hydroxy-3-methylbutyl)-7-methoxycoumarin (5) which on reaction with sodium borohydride affords osthol epoxide (7) (meranzin).The epoxide 7 is converted back into the bromohydrin 5 by the action of HBr in dioxane and to 8-(2-amino-3-hydroxy-3-methylbutyl)-7-methoxycoumarin (8) by the action of ammonia.

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