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(3-Isopropyl-isoxazol-5-yl)-methanol is a chemical compound characterized by the molecular formula C8H11NO2. It is an isoxazole derivative that features a hydroxyl group, classifying it as an alcohol. (3-Isopropyl-isoxazol-5-yl)-methanol is primarily utilized as a synthetic building block for the creation of other chemicals and pharmaceuticals. Its potential extends to the realm of medicinal chemistry and drug discovery, where it may contribute to the development of novel therapeutic agents. However, it is crucial to handle and store (3-Isopropyl-isoxazol-5-yl)-methanol with care due to the health and safety risks it may present if mismanaged.

14633-17-1

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14633-17-1 Usage

Uses

Used in Pharmaceutical Synthesis:
(3-Isopropyl-isoxazol-5-yl)-methanol is used as a synthetic intermediate for the development of various pharmaceuticals. Its unique structure allows it to be a key component in the synthesis of new drugs, potentially leading to the discovery of innovative treatments for a range of medical conditions.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (3-Isopropyl-isoxazol-5-yl)-methanol is employed as a research tool to explore its properties and potential interactions with biological targets. This can aid in understanding its therapeutic potential and in designing new molecules with improved efficacy and safety profiles.
Used in Chemical Synthesis Industry:
(3-Isopropyl-isoxazol-5-yl)-methanol is used as a building block in the chemical synthesis industry for creating a variety of chemical compounds. Its versatility in chemical reactions makes it a valuable asset in the development of new chemical entities for various applications, including but not limited to materials science, agrochemicals, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 14633-17-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,3 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14633-17:
(7*1)+(6*4)+(5*6)+(4*3)+(3*3)+(2*1)+(1*7)=91
91 % 10 = 1
So 14633-17-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO2/c1-5(2)7-3-6(4-9)10-8-7/h3,5,9H,4H2,1-2H3

14633-17-1 Well-known Company Product Price

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  • Aldrich

  • (CBR00160)  (3-Isopropylisoxazol-5-yl)methanol  AldrichCPR

  • 14633-17-1

  • CBR00160-1G

  • 3,221.01CNY

  • Detail

14633-17-1SDS

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 (3-propan-2-yl-1,2-oxazol-5-yl)methanol

1.2 Other means of identification

Product number -
Other names [3-(propan-2-yl)-1,2-oxazol-5-yl]methanol

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:14633-17-1 SDS

14633-17-1Relevant academic research and scientific papers

Novel pyrrolidine or piperidine derivatives having activity for T-type calcium channel

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Paragraph 0203-0206, (2020/04/23)

A pyrrolidine or piperidine compound having activity for T - type calcium channel, wherein the pyrrolidine or piperidine compound of Formula 1 according to the present invention has an excellent antagonistic activity to, T-type calcium channel, and can be used as a preventive or therapeutic agent, for pain diseases, or cancer related to cancer, or cancer such as, epilepsy and,hepatic pain, angina. (by machine translation)

HYDROXYL PURINE COMPOUNDS AND USE THEREOF

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Paragraph 0151; 0152; 0153; 0154, (2018/04/05)

Disclosed are a series of hydroxyl purine compounds and the use thereof as PDE2 or TNFα inhibitors, in particular, the compounds as shown in formula (I), or tautomers thereof or pharmaceutically acceptable salts thereof.

COMPOUNS, COMPOSITIONS AND METHODS OF USE

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Page/Page column 171; 172, (2018/07/29)

Herein, compounds, compositions and methods for modulating inclusion formation and stress granules in cells related to the onset of neurodegenerative diseases, musculoskeletal diseases, cancer, ophthalmological diseases, and viral infections are described.

Ramoplanin derivatives possessing antibacterial activity

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Page/Page column 39; 66, (2010/11/23)

Novel ramoplanin derivatives are disclosed. These ramoplanin derivatives exhibit antibacterial activity. As the compounds of the subject invention exhibit potent activities against gram positive bacteria, they are useful antimicrobial agents. Methods of synthesis and of use of the compounds are also disclosed.

RETROVIRAL PROTEASE INHIBITING COMPOUNDS

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, (2008/06/13)

A retroviral protease inhibiting compound of the formula: STR1 is disclosed wherein R 1, R 2, R 5, R 6, Y m and Y' n are herein defined.

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