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5987-00-8

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5987-00-8 Usage

General Description

4-(2,5-Dimethyl-1H-pyrrol-1-yl)-2-hydroxybenzoic acid is a chemical compound that contains a pyrrole ring and a benzoic acid group. It is commonly used as a building block in organic synthesis and as a reagent in various chemical reactions. 4-(2,5-DIMETHYL-1H-PYRROL-1-YL)-2-HYDROXYBENZOIC ACID has potential pharmacological properties and has been studied for its anti-inflammatory and anti-cancer activities. It is often used in medicinal chemistry research for developing new drugs and pharmaceuticals. Additionally, it has been studied for its antioxidant properties and potential applications in the food and cosmetic industries.

Check Digit Verification of cas no

The CAS Registry Mumber 5987-00-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,8 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5987-00:
(6*5)+(5*9)+(4*8)+(3*7)+(2*0)+(1*0)=128
128 % 10 = 8
So 5987-00-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H13NO3/c1-8-3-4-9(2)14(8)10-5-6-11(13(16)17)12(15)7-10/h3-7,15H,1-2H3,(H,16,17)

5987-00-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2,5-Dimethyl-pyrrol-1-yl)-2-hydroxy-benzoic acid

1.2 Other means of identification

Product number -
Other names 16-Monoacetyl-diginatigenin

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:5987-00-8 SDS

5987-00-8Downstream Products

5987-00-8Relevant articles and documents

Synthesis and biological activity of 16β-morpholinosteroid derivatives

Piplani,Jindal,Fajrak,Prior,Marshall

, p. 363 - 367 (2007/10/03)

Fusion of morpholine at the 16 position of the steroid nucleus has been carried out to prepare monoquaternary 6,7 and 8 and bisquaternary ammonium compounds 13 and 14. Compounds 13 and 14 partly resemble chandonium iodide in structure. All the compounds have been evaluated for their neuromuscular blocking and ganglion blocking activities. The compounds 3, 4, 5, 11 and 12 have been screened for antineoplastic activity at NCI, Bethesda.

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