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(3-Propyl-isoxazol-5-yl)-methanol is a chemical compound with the molecular formula C8H11NO2. It belongs to the class of isoxazole derivatives and is commonly used in pharmaceutical research as a building block for the synthesis of various bioactive compounds. Its structure consists of a propyl chain attached to an isoxazole ring, with a hydroxyl group (-OH) attached to the isoxazole ring. (3-Propyl-isoxazol-5-yl)-methanol has potential pharmacological properties and is being studied for its potential use in the treatment of various diseases and disorders. Due to its unique structure and potential therapeutic properties, (3-Propyl-isoxazol-5-yl)-methanol is a subject of ongoing research and interest in the scientific community.

14716-91-7

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14716-91-7 Usage

Uses

Used in Pharmaceutical Research:
(3-Propyl-isoxazol-5-yl)-methanol is used as a building block for the synthesis of various bioactive compounds for the development of new drugs.
Used in Chemical Biology and Medicinal Chemistry:
(3-Propyl-isoxazol-5-yl)-methanol is used as a research compound to study its potential pharmacological properties and explore its applications in the treatment of various diseases and disorders.
Used in Drug Development:
(3-Propyl-isoxazol-5-yl)-methanol is used as a starting material for the development of new drugs with potential therapeutic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 14716-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,1 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14716-91:
(7*1)+(6*4)+(5*7)+(4*1)+(3*6)+(2*9)+(1*1)=107
107 % 10 = 7
So 14716-91-7 is a valid CAS Registry Number.

14716-91-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-propylisoxazol-5-yl)methanol

1.2 Other means of identification

Product number -
Other names 3-(n-Propyl)-5-hydroxymethyl-isoxazol

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:14716-91-7 SDS

14716-91-7Downstream Products

14716-91-7Relevant academic research and scientific papers

A method for generating nitrile oxides from nitroalkanes: A microwave assisted route for isoxazoles

Giacomelli, Giampaolo,De Luca, Lidia,Porcheddu, Andrea

, p. 5437 - 5440 (2007/10/03)

A convenient route has been developed for generation of nitrile oxides in situ from nitroalkanes under very mild conditions using microwave irradiation, using 4-(4,6-dimethoxy[1,3,5]triazin-2-yl)-4-methylmorpholinium chloride (DMTMM) and DMAP as catalyst.

A strategic alternative to solid phase synthesis: Preparation of a small isoxazoline library by 'fluorous synthesis'

Studer, Armido,Curran, Dennis P.

, p. 6681 - 6696 (2007/10/03)

The preparation of a highly fluorinated silyl group and its use as a 'fluorous label' are described. Allyl and propargyl alcohols are rendered fluorous upon attachment to the fluorous label. Cycloaddition of the fluorous dipolarophiles to nitrile oxides provides the corresponding isoxazol(in)es which are purified by simple liquid-liquid extractions. After detachment of the label and renewed extraction, the organic isoxazol(in)es are obtained. This new fluorous methodology allows the preparation of isoxazol(in)es in high purities without using chromatography.

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