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5-[2-(benzyloxy)-5-(1-methylethyl)phenyl]-1H-pyrazol-3-amine is a complex organic compound with the molecular formula C20H21N3O. It features a pyrazole ring, which is a five-membered aromatic ring containing three nitrogen atoms, with one nitrogen atom at the 3-position being part of an amino group. The compound also includes a benzyloxy group attached to a phenyl ring, which is further substituted with a 1-methylethyl (isopropyl) group at the 5-position. This chemical structure is significant in the field of medicinal chemistry, as it may exhibit biological activity or serve as a building block for the synthesis of pharmaceuticals. The specific properties and applications of 5-[2-(benzyloxy)-5-(1-methylethyl)phenyl]-1H-pyrazol-3-amine would depend on its ability to interact with biological targets, such as enzymes or receptors, which could make it a potential candidate for drug development.

4981-07-1

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4981-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4981-07-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,8 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4981-07:
(6*4)+(5*9)+(4*8)+(3*1)+(2*0)+(1*7)=111
111 % 10 = 1
So 4981-07-1 is a valid CAS Registry Number.

4981-07-1SDS

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 5-(2-phenylmethoxy-5-propan-2-ylphenyl)-1H-pyrazol-3-amine

1.2 Other means of identification

Product number -
Other names -

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

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More Details:4981-07-1 SDS

4981-07-1Downstream Products

4981-07-1Relevant academic research and scientific papers

Synthesis and antibacterial/antitubercular activity evaluation of symmetrical trans-cyclohexane-1,4-diamine derivatives

Kumar, Nitin,Kapoor, Ekta,Singh, Ramandeep,Kidwai, Saqib,Kumbukgolla, Widuranga,Bhagat, Sunita,Rawat, Diwan S

, p. 1441 - 1450 (2014/01/06)

A library of symmetrical trans-cyclohexane-1,4-diamine derivatives have been synthesized and evaluated for their activity against the M. tb H 37Rv strain. Most of the synthesized compounds show moderate to weak activity against M. tb H37Rv strain. Out of twenty-seven compounds tested, four compounds having substitution at p-position on the aromatic ring exhibit activity with MIC99 value ranging from 12.5 -25 μM. Compound 9u having i-propyl group substitution at p-position is found to be the most potent among all the tested compounds with MIC99 value of 12.5 μM against M. tb H37Rv strain. All these compounds have also been tested against Methicilin resistant Staphylococcus aureus (MRSA), and four of the compounds 9c, 9i, 9p and 9s possess good antibacterial activity with IC 50 ranging from 128 mg/L -256 mg/L.

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