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1,2-Benzisoxazol-3-amine,6-chloro-(9CI) is a chemical compound characterized by the presence of a benzisoxazole ring, an amino group, and a chlorine atom. It has a molecular formula of C7H6ClN3O and a molecular weight of 175.59 g/mol. 1,2-Benzisoxazol-3-amine,6-chloro-(9CI) may be utilized in the synthesis of pharmaceuticals or as a reagent in various chemical reactions. Due to its potential hazards, it is essential to handle and store 1,2-Benzisoxazol-3-amine,6-chloro-(9CI) according to proper safety protocols.

89692-53-5

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89692-53-5 Usage

Uses

Used in Pharmaceutical Synthesis:
1,2-Benzisoxazol-3-amine,6-chloro-(9CI) is used as a key intermediate in the synthesis of pharmaceuticals for its unique chemical structure and reactivity. Its presence in the molecular framework can contribute to the development of new drugs with specific therapeutic properties.
Used in Chemical Reactions as a Reagent:
In the field of organic chemistry, 1,2-Benzisoxazol-3-amine,6-chloro-(9CI) serves as a reagent in various chemical reactions, facilitating the formation of desired products. Its versatility in reacting with different types of compounds makes it a valuable asset in the synthesis of complex organic molecules.
Used in Research and Development:
1,2-Benzisoxazol-3-amine,6-chloro-(9CI) is utilized in research and development for exploring its potential applications and properties. Scientists and researchers investigate its chemical behavior, reactivity, and possible uses in creating new compounds or improving existing ones.
Used in Analytical Chemistry:
In analytical chemistry, 1,2-Benzisoxazol-3-amine,6-chloro-(9CI) may be employed as a reference compound or a standard for calibration in various analytical techniques. Its distinct chemical properties can aid in the accurate measurement and analysis of other compounds.
Used in Material Science:
1,2-Benzisoxazol-3-amine,6-chloro-(9CI) can be incorporated into the development of new materials with specific properties, such as improved stability, reactivity, or selectivity. Its unique structure and functional groups can contribute to the creation of advanced materials for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 89692-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,9 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89692-53:
(7*8)+(6*9)+(5*6)+(4*9)+(3*2)+(2*5)+(1*3)=195
195 % 10 = 5
So 89692-53-5 is a valid CAS Registry Number.

89692-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-1,2-benzoxazol-3-amine

1.2 Other means of identification

Product number -
Other names 6-chlorobenzo[d]isoxazol-3-amine

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:89692-53-5 SDS

89692-53-5Downstream Products

89692-53-5Relevant academic research and scientific papers

GEMINAL SUBSTITUTED AMINOBENZISOXAZOLE COMPOUNDS AS AGONISTS OF α7-NICOTINIC ACETYLCHOLINE RECEPTORS

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Paragraph 00256; 00257, (2017/03/08)

The present invention relates to novel geminal substituted aminobenzisoxazole compounds, and pharmaceutical compositions of the same, that are suitable as agonists or partial agonists of α7- nAChR, and methods of preparing these compounds and compositions

AMINOBENZISOXAZOLE COMPOUNDS AS AGONISTS OF A7-NICOTINIC ACETYLCHOLINE RECEPTORS

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Paragraph 00195, (2017/01/31)

The present invention relates to novel aminobenzisoxazole compounds, and pharmaceutical compositions of the same, that are suitable as agonists or partial agonists of ot7-nAChR, and methods of preparing these compounds and compositions, and the use of these compounds and compositions in methods of maintaining, treating and/or improving cognitive function. In particular, methods of administering the compound or composition to a patient in need thereof, for example a patient with a cognitive deficiency and/or a desire to enhance cognitive function, that may derive a benefit therefrom.

Novel one-pot cyclization of ortho substituted benzonitriles to 3-amino-1,2-benzisoxazoles

Palermo

, p. 2885 - 2886 (2007/10/03)

A novel one-pot synthesis of 3-amino-1,2-benzisoxazoles (iii), from ortho substituted benzonitriles (i), is described. The synthesis likely involves a SNAr reaction of an activated ortho halo or nitro group by a hydroxamate anion, followed by an intra-mol

SUBSTITUTED (PYRIDINYLAMINO)-INDOLES

-

, (2008/06/13)

There are disclosed various compounds of the formula below, STR1 where R, R 1, W, X, Y and Z are as defined in the specification; which are useful for alleviating various memory dysfunctions such as Alzheimer's disease, as modulators of neurotransmitter f

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