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112789-90-9

7-Methoxy-8-[(E)-3-oxo-1-butenyl]-2H-1-benzopyran-2-one, commonly known as umbelliferone, is a naturally occurring coumarin compound found in various plant sources such as Angelica archangelica and citrus fruits. It is recognized for its antioxidant and anti-inflammatory properties, as well as its potential health benefits, including protection against UV radiation damage, reduction of inflammation, and antitumor and antimicrobial activities.

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  • 112789-90-9 Structure

  • Basic information

    1. Product Name: 7-Methoxy-8-[(E)-3-oxo-1-butenyl]-2H-1-benzopyran-2-one
    2. Synonyms: 7-Methoxy-8-[(E)-3-oxo-1-butenyl]-2H-1-benzopyran-2-one;Osthenone;7-Methoxy-8-[(1E)-3-oxo-1-butenyl]-2H-1-benzopyran-2-one;Osthenon
    3. CAS NO:112789-90-9
    4. Molecular Formula: C14H12O4
    5. Molecular Weight: 244.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112789-90-9.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-[(E)-3-oxo-1-butenyl]-2H-1-benzopyran-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-Methoxy-8-[(E)-3-oxo-1-butenyl]-2H-1-benzopyran-2-one(112789-90-9)
    11. EPA Substance Registry System: 7-Methoxy-8-[(E)-3-oxo-1-butenyl]-2H-1-benzopyran-2-one(112789-90-9)

  • 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: 112789-90-9(Hazardous Substances Data)

112789-90-9 Usage

Uses

Used in Pharmaceutical Industry:
Umbelliferone is used as a therapeutic agent for its anti-inflammatory and antioxidant properties, which can help in the treatment of various inflammatory and oxidative stress-related conditions.
Used in Cosmetics Industry:
In the cosmetics industry, umbelliferone is used as an active ingredient in skincare products for its potential benefits in treating various skin conditions, such as acne and aging, due to its antioxidant and anti-inflammatory properties.
Used in Food Industry:
Umbelliferone is used as a natural food preservative, leveraging its antioxidant properties to extend the shelf life of food products and protect them from spoilage and oxidation.
Used in Antimicrobial Applications:
Due to its antimicrobial activity, umbelliferone is used in various applications to inhibit the growth of harmful microorganisms, such as in the development of antimicrobial coatings or in the formulation of natural disinfectants.
Used in Antitumor Applications:
Umbelliferone has been studied for its potential antitumor activity, and it is used in research and development for the treatment of cancer, as it may help in inhibiting tumor growth and reducing the risk of cancer progression.

Check Digit Verification of cas no

The CAS Registry Mumber 112789-90-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,7,8 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112789-90:
(8*1)+(7*1)+(6*2)+(5*7)+(4*8)+(3*9)+(2*9)+(1*0)=139
139 % 10 = 9
So 112789-90-9 is a valid CAS Registry Number.

112789-90-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Methoxy-8-[(1E)-3-oxo-1-buten-1-yl]-2H-chromen-2-one

1.2 Other means of identification

Product number -
Other names 7-Octadecenoic acid

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:112789-90-9 SDS

112789-90-9Downstream Products

112789-90-9Relevant articles and documents

A route to the structure proposed for puetuberosanol and approaches to the natural products marshrin and phebalosin

Gillmore, Adam,Lauret, Christelle,Roberts, Stanley M.

, p. 4363 - 4375 (2007/10/03)

Synthesis of the structure claimed for puetuberosanol 1 (using the Juliá-Colonna oxidation in a key step) showed that the natural product was a different material. The isomeric epoxy alcohols 16-18 can be discounted from the alternatives. An analogue 19 of marshrin 2 was prepared but the synthesis of the natural product was thwarted by failure of a Juliá-Colonna oxidation in the key step. The epoxy ketone 29 was prepared by Darzens condensation and was converted into (±)-phebalosin 3.

Structure of bisosthenon, a novel dimeric coumarin from Citrus plants

Ito, Chihiro,Ju-ichi, Motoharu,Inoue, Mami,Muraguchi, Miki,Mizuno, Toyoko,et al.

, p. 1957 - 1959 (2007/10/02)

A new dimeric coumarin, named bisosthenon (1), was isolated from the roots of some Citrus plants.The strucure 1, corresponding to a head-to-head dimer of osthenon (4), prviously obtained from Citrus plants, was eluciated by spectrometric and X-ray analysis.The photodimerization of 4 was also studied.Keywords - coumarin; Rutaceae; Citrus; bisosthenon; osthenon; photodimerization; dimer; cyclobutane; X-ray.

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