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1H-Indole, 3-(4,5-dihydro-3-phenyl-5-isoxazolyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69022-92-0

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69022-92-0 Usage

Chemical Class

The compound belongs to the indole class of compounds.

Structural Features

The compound contains a phenyl group and an isoxazolyl group, which are important structural features in medicinal chemistry.

Biological Activity

Indole compounds are often found in natural products and have various biological activities, suggesting that 1H-Indole, 3-(4,5-dihydro-3-phenyl-5-isoxazolyl)- might possess significant biological activity.

Potential Pharmacological Effects

The presence of important structural features in medicinal chemistry suggests that 1H-Indole, 3-(4,5-dihydro-3-phenyl-5-isoxazolyl)- might have potential pharmacological effects.

New Drug Development

Further research and investigation into the properties and potential applications of 1H-Indole, 3-(4,5-dihydro-3-phenyl-5-isoxazolyl)- could lead to the development of new drugs or therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 69022-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,2 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69022-92:
(7*6)+(6*9)+(5*0)+(4*2)+(3*2)+(2*9)+(1*2)=130
130 % 10 = 0
So 69022-92-0 is a valid CAS Registry Number.

69022-92-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(1H-indol-3-yl)-3-phenyl-4,5-dihydro-1,2-oxazole

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:69022-92-0 SDS

69022-92-0Relevant academic research and scientific papers

An efficient method for the synthesis of isoxazolines under microwave irradiation and solvent-free conditions

Patil, Pravin O.,Bari, Sanjay B.

, p. 3588 - 3590 (2013/04/24)

A facile method for the synthesis of new isoxazoline derivatives are being reported starting from substituted 1-(1H-indol-3-yl)-3-(substituted aryl)-prop-1-en-3-ones and hydroxylamine hydrochloride under solvent free conditions and microwave irradiation.

Design and synthesis of 3-[3-(substituted phenyl)-4-piperidin-1-ylmethyl/- 4-morpholin-4-ylmethyl-4,5-dihydro-isoxazol-5-yl]-1H-indoles as potent anti-inflammatory agents

Amir, Mohammad,Javed, Sadique Akhtar,Kumar, Harish

, p. 299 - 310 (2011/01/12)

The synthesis of new indole derivatives bearing isoxazoline moiety (3a-d and 4a-d) has been described. IR, 1H NMR, and mass spectral data supported the structures of synthesized compounds. The compounds were tested in vivo for their anti-inflam

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