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8-METHOXY-4-METHYLBENZO[G]COUMARIN is a coumarin derivative with a molecular formula C17H14O3. It is known for its anticoagulant and antioxidant properties and has been studied for its potential use as a fluorescent probe in analytical chemistry, as well as in the development of new drugs. 8-METHOXY-4-METHYLBENZO[G]COUMARIN has also been investigated for its potential anti-cancer and anti-inflammatory properties, making it a subject of interest in pharmaceutical research. Its potent antioxidant activity is important for its potential use in the development of new therapeutic agents for a variety of medical conditions.

69169-71-7

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69169-71-7 Usage

Uses

Used in Pharmaceutical Research:
8-METHOXY-4-METHYLBENZO[G]COUMARIN is used as a potential anti-cancer and anti-inflammatory agent for its potential therapeutic effects in treating various medical conditions.
Used in Analytical Chemistry:
8-METHOXY-4-METHYLBENZO[G]COUMARIN is used as a fluorescent probe for its potential applications in analytical chemistry.
Used in Drug Development:
8-METHOXY-4-METHYLBENZO[G]COUMARIN is used in the development of new drugs due to its potent antioxidant activity and potential therapeutic effects.

Check Digit Verification of cas no

The CAS Registry Mumber 69169-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,1,6 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69169-71:
(7*6)+(6*9)+(5*1)+(4*6)+(3*9)+(2*7)+(1*1)=167
167 % 10 = 7
So 69169-71-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H12O3/c1-9-5-15(16)18-14-8-11-6-12(17-2)4-3-10(11)7-13(9)14/h3-8H,1-2H3

69169-71-7SDS

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 8-methoxy-4-methylbenzo[g]chromen-2-one

1.2 Other means of identification

Product number -
Other names M1862

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:69169-71-7 SDS

69169-71-7Downstream Products

69169-71-7Relevant academic research and scientific papers

Environment-sensitive fluorophore emitting in protic environments

Uchiyama, Seiichi,Takehira, Kazuyuki,Yoshihara, Toshitada,Tobita, Seiji,Ohwada, Tomohiko

, p. 5869 - 5872 (2006)

(Diagram presented) The unusual fluorescence properties of 8-methoxy-4-methyl-2H-benzo[g]chromen-2-one (1) are described. The fluorophore 1 is almost nonfluorescent in aprotic solvent (e.g., fluorescence quantum yield Φf 450 nm) in protic solvent (e.g., Φf = 0.21 in methanol). The fluorophore 1 also shows good applicability in developing a new fluorogenic (fluorescent "off-on") sensor.

Comparative study of polyaromatic and polyheteroaromatic fluorescent photocleavable protecting groups

Fernandes, Maria J.G.,Gon?alves, M. Sameiro T.,Costa, Susana P.G.

, p. 3032 - 3038 (2008/09/19)

Fluorescent conjugates of N-benzyloxycarbonyl protected γ-aminobutyric acid were prepared by coupling to its C-terminus several polyheteroaromatic, based on the oxobenzopyran skeleton (trivially known as coumarin) and polyaromatic labels, such as naphthalene and pyrene. Photophysical properties were evaluated, as well as their behaviour towards photocleavage by irradiation in MeOH/HEPES buffer solution (80:20), in a photochemical reactor at different wavelengths (254, 300, 350 and 419 nm), followed by HPLC/UV monitoring.

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