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CAS

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737-52-0

Oxypeucedanin, a derivative of Psoralen, is a phytoalexin compound found in various plant species. It plays a crucial role in the plant's defense mechanism against fungal and insect attacks. Additionally, it exhibits photosensitizing and phototoxic properties, making it a valuable component in photochemotherapy and as a photochemical probe in biological systems.

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  • 737-52-0 Structure

  • Basic information

    1. Product Name: OXYPEUCEDANIN
    2. Synonyms: OXYPEUCEDANIN;oxypeucadanin;4-(3,3-Dimethylglycidyloxy)-7H-furo[3,2-g][1]benzopyran-7-one;4-(3,3-Dimethyloxiran-2-ylmethoxy)-7H-furo[3,2-g][1]benzopyran-7-one;4-[(3,3-Dimethyloxiranyl)methoxy]-7H-furo[3,2-g][1]benzopyran-7-one;Oxypencedanin;4-[(3,3-dimethyloxiran-2-yl)methoxy]furo[3,2-g]chromen-7-one;Oxypeucedanin, 98%, from Angelica biserrata (Shan & C. Q. Yuan) C. Q. Yuan & Shan
    3. CAS NO:737-52-0
    4. Molecular Formula: C16H14O5
    5. Molecular Weight: 286.28
    6. EINECS: N/A
    7. Product Categories: Coumarins
    8. Mol File: 737-52-0.mol

  • Chemical Properties

    1. Melting Point: 141-142 °C
    2. Boiling Point: 469.6oC at 760 mmHg
    3. Flash Point: 237.8oC
    4. Appearance: /
    5. Density: 1.36g/cm3
    6. Vapor Pressure: 5.41E-09mmHg at 25°C
    7. Refractive Index: 1.633
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: OXYPEUCEDANIN(CAS DataBase Reference)
    11. NIST Chemistry Reference: OXYPEUCEDANIN(737-52-0)
    12. EPA Substance Registry System: OXYPEUCEDANIN(737-52-0)

  • 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: 737-52-0(Hazardous Substances Data)

737-52-0 Usage

Uses

Used in Photochemotherapy:
Oxypeucedanin is used as a photochemotherapeutic agent for the management of skin conditions such as vitiligo, psoriasis, and mycosis fungoides. Its photosensitizing properties enable it to effectively target and treat these conditions when combined with light exposure.
Used as a Photochemical Probe in Biological Systems:
Oxypeucedanin serves as a valuable tool in biological research, acting as a photochemical probe to study various cellular processes and interactions. Its ability to bind and interact with biomolecules allows researchers to gain insights into the mechanisms of action and potential applications in different biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 737-52-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 737-52:
(5*7)+(4*3)+(3*7)+(2*5)+(1*2)=80
80 % 10 = 0
So 737-52-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H14O5/c1-16(2)14(21-16)8-19-12-7-15(17)20-13-6-11-9(3-4-18-11)5-10(12)13/h3-7,14H,8H2,1-2H3

737-52-0SDS

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 OXYPEUCEDANIN

1.2 Other means of identification

Product number -
Other names oxypeucadanin

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:737-52-0 SDS

737-52-0Relevant articles and documents

Design, synthesis and evaluation of furanocoumarin monomers as inhibitors of CYP3A4

Row,Brown,Stachulski,Lennard

, p. 1604 - 1610 (2008/02/03)

A number of furanocoumarins isolated from grapefruit juice have been found to inhibit CYP3A4 activity in vitro. In this study, we have designed and synthesised a range of analogues based on bergamottin to investigate the relationship between chemical stru

Resolution of prenyl bromohydrin esters and derivatives: Synthesis of the quinoline alkaloid (+)-(R)- and (-)-(S)-lunacridine

Barr,Boyd,Sharma,Evans,Malone,Mehta

, p. 11219 - 11234 (2007/10/02)

Chromatographic separation of the bromohydrin MTPA diastereoisomers formed at the prenyl group attached to quinoline and coumarin rings is reported; base catalysed cyclization of the bromo MTPA esters in the quinoline series yielded the corresponding pren

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