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38873-55-1

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38873-55-1 Usage

Uses

nti-inflammatory.

Check Digit Verification of cas no

The CAS Registry Mumber 38873-55-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,7 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38873-55:
(7*3)+(6*8)+(5*8)+(4*7)+(3*3)+(2*5)+(1*5)=161
161 % 10 = 1
So 38873-55-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H12O4/c17-13(6-8-16(18)19)10-5-7-15-12(9-10)11-3-1-2-4-14(11)20-15/h1-5,7,9H,6,8H2,(H,18,19)

38873-55-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-dibenzofuran-2-yl-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names 4-dibenzofuran-2-yl-4-oxo-butyric acid

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:38873-55-1 SDS

38873-55-1Relevant academic research and scientific papers

Tricyclic inhibitor of matrix metalloproteinases

-

, (2008/06/13)

A tricyclic compound is described as well as pharmaceutical compositions of same, which is useful as an inhibitor of matrix metalloproteinases, particularly gelatinase A (72 kD gelatinase) for the treatment of multiple sclerosis or other autoimmune or inflammatory disorders dependent upon tissue invasion by leukocytes.

Purification of γ-oxo-2-dibenzofuranbutyric acid

-

, (2008/06/13)

A process for the separation of γ-oxo-2-dibenzofuranbutyric acid from a mixture of said acid and γ-oxo-3-dibenzofuranbutyric acid is disclosed. Such a mixture is obtained by the prior art method of preparing γ-oxo-2-dibenzofuranbutyric acid from dibenzofuran and succinic anhydride in a Friedel-Crafts reaction. The mixture of acids is converted to a mixture of their corresponding lower alkyl esters which is separated by recrystallization or chromatography into its component alkyl esters. Hydrolysis of the lower alkyl ester of γ-oxo-2-dibenzofuranbutyric acid gives the desired corresponding acid.

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