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2,3-dihydro-5-methoxy-6-Benzofurancarboxaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99355-75-6

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99355-75-6 Usage

Compound type

Chemical compound

Derivative

Benzofuran

Usage

Synthesis of various pharmaceutical compounds

Physical appearance

White solid

Odor

Sweet, floral

Application

Fragrance ingredient in perfumes and cosmetic products

Utilization

Production of flavoring agents

Role

Precursor in the synthesis of other organic compounds

Pharmacological activity

Potential applications in the development of new drugs and pharmaceutical products

Check Digit Verification of cas no

The CAS Registry Mumber 99355-75-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,5 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 99355-75:
(7*9)+(6*9)+(5*3)+(4*5)+(3*5)+(2*7)+(1*5)=186
186 % 10 = 6
So 99355-75-6 is a valid CAS Registry Number.

99355-75-6SDS

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 5-Methoxy-2,3-dihydro-1-benzofuran-6-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2,3-Dimethyl-5-methoxyphenol

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:99355-75-6 SDS

99355-75-6Relevant academic research and scientific papers

ENDOTHELIN RECEPTOR ANTAGONISTS

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Page column 21, (2008/06/13)

Novel pyrroles, pyrazoles and triazoles, pharmaceutical compositions containing these compounds and their use as endothelin receptor antagonists are described.

A practical approach to highly functionalized benzodihydrofurans

Plotkin, Michael,Chen, Sanyou,Spoors, P. Grant

, p. 2269 - 2273 (2007/10/03)

A number of aromatic dibromides have been treated with 2-3 equivalents of n-butyllithium in order to initiate two sequential chemical events, a Parham cyclization and an intermolecular reaction with DMF. (C) 2000 Elsevier Science Ltd.

ENDOTHELIN RECEPTOR ANTAGONISTS

-

, (2008/06/13)

Novel pyrroles, pyrazoles and triazoles, pharmaceutical compositions containing these compounds and their use as endothelin receptor antagonists are described.

Relevance of Conformational Constraints to the Regioselective Lithiation of Aromatic Diethers. Application to the Convenient Construction of the DEF Tricyclic Subunit of the Austalides

Paquette, Leo A.,Schulze, Matthias M.,Bolin, David G.

, p. 2043 - 2051 (2007/10/02)

The lithiation of 29 and 30 is shown to occur at all three sites with a dissimilar kinetic preference.For the dihydrofuran, reaction at the proton labeled Hβ' operates predominantly; in the dihydropyran example, Hα is the favored sit

Antioxidant-Based Inhibitors of Leukotriene Biosynthesis. The Discovery of 6--1-propen-3-yl>-2,3-dihydro-5-benzofuranol, a Potent Topical Antiinflammatory Agent

Hammond, Milton L.,Zambias, Robert A.,Chang, Michael N.,Jensen, Norman P.,McDonald, John,et al.

, p. 909 - 918 (2007/10/02)

The leukotrienes, metabolites of arachidonic acid produced through the action of the enzyme 5-lipoxygenase, are important mediators of immediate hypersensitivity and inflammation.Among the variety of diseases in which the leukotrienes may play a symptomat

Synthesis and Evaluation of 2,3-Dihydrobenzofuran Analogues of the Hallucinogen 1-(2,5-Dimethoxy-4-methylphenyl)-2-aminopropane: Drug Discrimination Studies in Rats

Nichols, David E.,Hoffman, Andrew J.,Oberlender, Robert A.,Riggs, Robert M.

, p. 302 - 304 (2007/10/02)

Two analogues, 6-(2-aminopropyl)-5-methoxy-2,3-dihydrobenzofuran and 6-(2-aminopropyl)-5-methoxy-2-methyl-2,3-dihydrobenzofuran, of the hallucinogenic agent 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane (DOM) were synthesized and tested in the two-lever drug discrimination paradigm.In rats trained to discriminate saline from LSD tartrate (0.08 mg/kg), stimulus generalization occurred to both of the 2,3-dihydrobenzofuran analogues but at doses more than 10-fold higher than for DOM.A possible explanation for this dramatic attenuation of LSD-like activity could involve a highly directional electrophilic binding site on the receptor that cannot accept the orientation of the unshared electron pairs on the heterocyclic oxygen atom in the benzofurans.

Substituted 5-hydroxy-2,3-dihydrobenzofurans and analogs thereof useful as anti-inflammatory agents

-

, (2008/06/13)

Substituted 5-hydroxy-2,3-dihydrobenzofuran and analogs such as the substituted 6-hydroxy-2,3-dihydrobenzopyrans were prepared from an appropriately substituted (5-hydroxy-2,3-dihydrobenzofuran-6-yl) formaldehyde or analog thereof with an aryl amine follo

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