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5-butyl-7-methoxy-1-benzofuran-4-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99107-50-3

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99107-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99107-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,1,0 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 99107-50:
(7*9)+(6*9)+(5*1)+(4*0)+(3*7)+(2*5)+(1*0)=153
153 % 10 = 3
So 99107-50-3 is a valid CAS Registry Number.

99107-50-3SDS

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-butyl-7-methoxy-1-benzofuran-4-ol

1.2 Other means of identification

Product number -
Other names 5-butyl-7-methoxy-benzofuran-4-ol

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:99107-50-3 SDS

99107-50-3Upstream product

99107-50-3Relevant academic research and scientific papers

Substituted naphthalenes, indoles, benzofurans and benzothiophenes as lipoxygenase inhibitors

-

, (2008/06/13)

The present invention relates to substituted naphthalenes, indoles, benzofurans and benzothiophenes (many of which are novel) which are useful as inhibitors of the synthesis of leukotrienes and as inhibitors of the action of lipoxygenase in mammalian metabolism

1,4-Dihydronaphthoquinones, hydroindoloquinones, benzofurans, and benzothiophenes as inhibitors of 5-lipoxygenase. Synthesis and structure-activity studies

Yamashita,Schaub,Back,White,Toy,Ghazal,Burdick,Brashler,Holm

, p. 775 - 781 (2007/10/02)

A series of substituted 1,4-dihydronaphthoquinones, hydroindoloquinones, benzofuran-4,7-dihydroquinones, and benzothiophene-4,7-dihydroquinones were synthesized and evaluated for inhibitory activity against 5-lipoxygenase. These compounds were found to be active in vitro for LTC4/D4 inhibition with the potencies (IC50's) ranging from 0.2 to 85 μM. Active 1,4-dihydronaphthoquinone acetates (IC50 4 inhibition assay. The acetates of 1,4-dihydronaphthoquinones containing the alkyl substituent(s) (2-n-butyl, 11, and 2,3-diethyl, 15) exhibited the best activity in LTC4/D4 inhibition (IC50 = 0.2-0.4 μM, in vitro) as well as in LTB4 inhibition (60-75% inhibition).

REACTION OF ARYL CHROMIUM CARBENE COMPLEXES WITH 1-HEXYNE; FORMATION OF UNUSUAL DIELS-ALDER CYCLOADDITION PRODUCTS

Yamashita, A.,Timko, J.M.,Watt, W.

, p. 2513 - 2516 (2007/10/02)

The reaction of an aryl chromium carbene complex with 1-hexyne provided a benzannualated product as a major component along with unusual Diels-Alder cycloaddition products.

Substituted naphthalenes, indoles, benzofurans, and benzothiophenes as lipoxygenase inhibitors

-

, (2008/06/13)

The present invention provides certain novel substituted naphthalenes, indoles, benzofurans, and benzothiophenes of Formula I which are useful as inhibitors of leukotriene biosynthesis and as inhibitors of lipoxygenase. They are thus employed wherever it is medically necessary or desirable to inhibit these systems. STR1

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