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4-Isoxazolemethanol, 3-methyl-5-(1-methylethyl)-(9CI) is a chemical compound with the molecular formula C9H13NO2. It is a derivative of isoxazole, a heterocyclic compound containing a five-membered ring with one oxygen and one nitrogen atom. The compound features a 3-methyl group attached to the isoxazole ring, a 5-(1-methylethyl) substituent, and a hydroxymethyl group at the 4-position. This specific arrangement of functional groups gives the compound unique chemical properties and potential applications in various fields, such as pharmaceuticals or agrochemicals. However, further research and characterization are needed to fully understand its potential uses and properties.

99299-08-8

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99299-08-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99299-08-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,2,9 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 99299-08:
(7*9)+(6*9)+(5*2)+(4*9)+(3*9)+(2*0)+(1*8)=198
198 % 10 = 8
So 99299-08-8 is a valid CAS Registry Number.

99299-08-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-Isopropyl-3-methyl-isoxazol-4-yl)-methanol

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:99299-08-8 SDS

99299-08-8Downstream Products

99299-08-8Relevant academic research and scientific papers

Metalation of Isoxazolyloxazolines, a Facile Route to Functionally Complex Isoxazoles: Utility, Scope, and Comparison to Dianion Methodology

Natale, N. R.,McKenna, John I.,Niou, Chorng-Shyr,Borth, Mark,Hope, Hakon

, p. 5660 - 5666 (2007/10/02)

2-(5'-Alkylisoxazol-4'-yl)-Δ2-oxazoline was metalated at the C-5' alkyl group, and the lithio anion was quenched with a variety of electrophiles.Alkyl halides, aldehydes, and acylpyridinium salts were used as electrophiles.The lithio anion was oxygenated with MOOPH or N-(phenylsulfonyl)oxaziridene.The isoxazolyloxazoline system was converted to the isoxazolyl carboxylic acid, aldehyde, ketone, and chiral oxazoline.The isoxazolyloxazoline was formed, metalated, and deprotected in synthetically useful yields and represents a facile entry into functionally complex isoxazoles.To determine the necessity of the oxazoline protection/deprotection scheme, dianions of isoxazole-4-carboxylic acids were studied.The dianion method was found to be more efficient for simple alkyl halides, but limited in scope.

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