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29505-13-3

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29505-13-3 Usage

Physical State

Colorless liquid

Explanation

The compound is in a liquid state and is colorless, which means it does not have any visible color.

Explanation

The compound is used as a starting material or intermediate in the synthesis of various pharmaceuticals and agrochemicals, which are chemicals used in the medical and agricultural industries, respectively.

Explanation

The compound serves as a solvent, which is a substance capable of dissolving other substances, and as a reagent, which is a substance used to initiate a chemical reaction.

Explanation

Cytotoxic properties refer to the ability of a substance to kill or inhibit the growth of cells, which can be useful in the development of drugs that target cancer cells.

Explanation

Antifungal properties refer to the ability of a substance to inhibit the growth of fungi, which can be useful in the development of antifungal drugs.

Explanation

Due to its cytotoxic and antifungal properties, the compound is being studied for its potential use in the development of new drugs.

Explanation

The compound's photochemical and photophysical properties make it a candidate for use in the development of OLEDs, which are devices that emit light when an electric current is applied.

Explanation

Photochemical properties refer to the chemical reactions that occur when a substance is exposed to light, while photophysical properties refer to the physical properties that are influenced by light. These properties make the compound suitable for use in photochemical applications.

Applications

Building block in pharmaceuticals and agrochemicals

Utilization

Solvent and reagent in organic chemical reactions

Cytotoxic Properties

Exhibits potential cytotoxic properties

Antifungal Properties

Exhibits potential antifungal properties

Drug Development

Investigated for potential use in drug development

Photochemical Applications

Studied for potential use in organic light-emitting diodes (OLEDs)

Photophysical Properties

Exhibits photochemical and photophysical properties

Check Digit Verification of cas no

The CAS Registry Mumber 29505-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,0 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29505-13:
(7*2)+(6*9)+(5*5)+(4*0)+(3*5)+(2*1)+(1*3)=113
113 % 10 = 3
So 29505-13-3 is a valid CAS Registry Number.

29505-13-3SDS

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 1,2-BENZISOXAZOLE, 3,6-DIMETHYL-

1.2 Other means of identification

Product number -
Other names 3,6-Dimethyl-2,1-benzisoxazol

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:29505-13-3 SDS

29505-13-3Relevant articles and documents

Triflic anhydride: A mild reagent for highly efficient synthesis of 1,2-benzisoxazoles, isoxazolo, and isothiazolo quinolines without additive or base

Kalkhambkar, Rajesh G.,Yuvaraj

supporting information, p. 547 - 555 (2014/01/23)

The synthetic utility of trifluoromethanesulphonic anhydride (triflic anhydride, TA) without additive or base for the high-yielding synthesis of a wide variety of 1,2-benzisoxazoles from 2-hydroxyaryl aldoximes and ketoximes under mild conditions has been carried out for the first time. As a continuation of our study, syntheses of isoxazolo and isothiazolo quinolones have also been demonstrated using triflic anhydride under similar conditions. This method is simple and has benefits from the easy way to isolate the products in excellent yields.

A novel method for the highly efficient synthesis of 1,2-benzisoxazoles under neutral conditions using the Ph3P/DDQ system

Iranpoor, Nasser,Firouzabadi, Habib,Nowrouzi, Najmeh

, p. 8247 - 8250 (2007/10/03)

The use of Ph3P/DDQ offers a novel, neutral and highly efficient method for the efficient conversion of 2-hydroxyaryl aldoximes and ketoximes to 1,2-benzisoxazoles in excellent yields at room temperature.

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