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7-hydroxy-5,8-dimethoxy-2-methyl-4-oxo-4H-chromene-6-carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92611-82-0 Structure
  • Basic information

    1. Product Name: 7-hydroxy-5,8-dimethoxy-2-methyl-4-oxo-4H-chromene-6-carbaldehyde
    2. Synonyms:
    3. CAS NO:92611-82-0
    4. Molecular Formula: C13H12O6
    5. Molecular Weight: 264.2308
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92611-82-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 509.1°C at 760 mmHg
    3. Flash Point: 198.8°C
    4. Appearance: N/A
    5. Density: 1.367g/cm3
    6. Vapor Pressure: 5.5E-11mmHg at 25°C
    7. Refractive Index: 1.604
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 7-hydroxy-5,8-dimethoxy-2-methyl-4-oxo-4H-chromene-6-carbaldehyde(CAS DataBase Reference)
    11. NIST Chemistry Reference: 7-hydroxy-5,8-dimethoxy-2-methyl-4-oxo-4H-chromene-6-carbaldehyde(92611-82-0)
    12. EPA Substance Registry System: 7-hydroxy-5,8-dimethoxy-2-methyl-4-oxo-4H-chromene-6-carbaldehyde(92611-82-0)
  • 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: 92611-82-0(Hazardous Substances Data)

92611-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92611-82-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,6,1 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 92611-82:
(7*9)+(6*2)+(5*6)+(4*1)+(3*1)+(2*8)+(1*2)=130
130 % 10 = 0
So 92611-82-0 is a valid CAS Registry Number.

92611-82-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-hydroxy-5,8-dimethoxy-2-methyl-4-oxochromene-6-carbaldehyde

1.2 Other means of identification

Product number -
Other names 7-hydroxy-5,8-dimethoxy-2-methyl-4-oxo-4H-chromene-6-carbaldehyde

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:92611-82-0 SDS

92611-82-0Relevant articles and documents

Synthesis and anticoagulant, antipyretic and analgesic activities of some 4H-1-benzopyran-4-one derivatives

El-Diwani, Hoda I.,El-Sahrawi, Hend,Mahmoud, Sawsan S.,Miyase, Toshio

, p. 27 - 31 (2007/10/02)

New derivatives of 7-hydroxy-5,8-dimethoxy-2-methyl-4(H)-oxo-1-benzopyran-6-carboxaldehyde (2a) have been synthesized and tested for their anticoagulant, antipyretic and analgesic activities.Compounds 2a, b and 3a, c, d show significant anticoagulant effe

UV-A Photolysis of Khellin: Products and Reaction Mechanism

Caffieri, Sergio,Favretto, Donata

, p. 7059 - 7063 (2007/10/02)

Photolysis at 365 nm of khellin in various solvents was studied: the degradation rate strongly depends on solvent but not on polarity, since it is related to the singlet oxygen lifetime in each solvent.Eight products were isolated and characterized, some of which had previously been described as coming from chemical oxidation of khellin.Both facts support an oxic pathway for photolysis involving singlet oxygen and leading to unstable intermediates.These are rapidly decomposed by nucleophiles, suggesting possible interference - if they are also formed in vivo - with physiological processes during photochemotherapeutic treatment with khellin.

ORGANOPHOSPHORUS CHEMISTRY 25. THE UTILIZATION OF WITTIG REAGENTS IN LACTONE RING FORMATION. APPLICATION TO THE SYNTHESIS OF LINEAR FUROCOUMARINS AND PYRANOCOUMARINS

Atta, Sanaa M. S.,Hafez, Taghrid S.,Mahran, Mohamed R.

, p. 109 - 116 (2007/10/02)

A new and improved method for the preparation of linear furocoumarins (7a,b) and pyranocoumarins (10a,b) in high yields, is described.It depends upon reacting ylid-phosphoranes (5) with suitably substituted benzofuran-, (3) or the benzo-γ-pyrone-(4) moiety.Formation of the target compounds (7 and 10) is assumed to proceed via lactonization of cis alkyl α-hydroxycinnamate intermediates of types 6 and 9, respectively.The trans analogues 8 do not lactonize to 10 even upon heating in boiling toluene.The new compounds have been characterized by their spectroscopic data (IR, PMR, 13C NMR) and elementary analyses. Key words: Wittig-reaction; lactonization; preparation of linear furocoumarins, pyranocoumarins.

Oxymetalation of Khellin. Solvomercuration, Osmylation, and Palladium-Catalyzed Oxidation of the Furan Ring in Khellin. The Synthesis of Highly Oxygenated Chromones and 2-Substituted Furochromones

Gammill, Ronald B.,Nash, Sharon A.

, p. 3116 - 3123 (2007/10/02)

Oxidation of khellin with thallium(III) nitrate (TTN) in methanol results in the addition of two molecules of methanol across the 2,3-double bond in the furan ring.Oxidation of khellin with mercuric(II) nitrate (Hg(NO3)2) in aqueous THF followed by treatm

Catalytic Osmylation and Oxypalladation of Khellin. Two Useful Methods for Furan Ring Degradation. Replacement of the Furan Ring by an Isoxazole Ring.

Gammill, Ronald B.,Nash, Sharon A.

, p. 2953 - 2956 (2007/10/02)

Two oxidation reactions are described which result in the selective degradation of the furan ring in khellin.Conversion of these products to previously inaccessible analogues is described.

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