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AKOS AU36-M553 is a chemical compound primarily used as a catalyst in various industrial processes. It is a member of the AKOS catalyst series, which is known for its high performance and selectivity in catalyzing reactions. This particular compound is often employed in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. It is characterized by its ability to facilitate specific chemical transformations under mild conditions, which can lead to improved yields and reduced environmental impact. The compound's properties make it a valuable tool in the synthesis of complex molecules, contributing to the efficiency and sustainability of chemical manufacturing processes.

5180-87-0

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5180-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5180-87-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,8 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5180-87:
(6*5)+(5*1)+(4*8)+(3*0)+(2*8)+(1*7)=90
90 % 10 = 0
So 5180-87-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO3/c1-8-5-6-9-3-2-4-10(12(9)13-8)16-7-11(14)15/h2-6H,7H2,1H3,(H,14,15)

5180-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methylquinolin-8-yl)oxyacetic acid

1.2 Other means of identification

Product number -
Other names 2-(2-methyl-8-quinolyloxy)acetic 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:5180-87-0 SDS

5180-87-0Downstream Products

5180-87-0Relevant academic research and scientific papers

Synthesis and biological efficacy of novel piperazine analogues bearing quinoline and pyridine moieties

Al-Ghorbani,Rekha,Lakshmi Ranganatha,Prashanth,Veerabasappagowda,Khanum

, p. 554 - 561 (2015)

A series of novel piperazine analogues bearing quinolin-8-yloxy-butan-1-ones/pyridin-2-yloxyethanones were synthesized by a simple and convenient approach based on various substituted piperazine incorporating quinoline and pyridine moieties. The analogues were evaluated for in vitro antioxidant activity against 2,2-diphenyl-1-picrylhydrazyl (DPPH) and ferrous ion radical scavenging activities and anti-inflammatory activity by inhibition of Vipera russelli venom (PLA2) and gastric K+/H+-ATPase activities. Most of the title compounds exhibited promising activity. Best antioxidant and PLA2-inhibiting activities were found for piperazine analogues with phenyl and nitro phenyl groups, whereas methoxy group on phenyl piperazine indicated selectivity for the H+/K+-ATPase.

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