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2,1-Benzisoxazole,5-chloro-(7CI,8CI,9CI) is a chemical compound with the molecular formula C7H4ClNO. It belongs to the class of isoxazoles and contains a benzene ring fused to an oxazole ring with a chlorine atom attached to the 5th carbon. 2,1-Benzisoxazole,5-chloro-(7CI,8CI,9CI) is used as a building block in organic synthesis and as a starting material for the production of pharmaceuticals and agrochemicals. It also exhibits biological activity and has been studied for its potential applications in medicinal chemistry. It is important to handle this chemical with care as it may pose health and environmental risks if not used and disposed of properly.

4596-92-3

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4596-92-3 Usage

Uses

Used in Pharmaceutical Industry:
2,1-Benzisoxazole,5-chloro-(7CI,8CI,9CI) is used as a building block in organic synthesis for the development of new pharmaceuticals. Its unique structure and biological activity make it a valuable component in the creation of novel drug candidates.
Used in Agrochemical Industry:
2,1-Benzisoxazole,5-chloro-(7CI,8CI,9CI) is used as a starting material for the production of agrochemicals. Its chemical properties and potential applications in this field contribute to the development of new products for agricultural use.
Used in Medicinal Chemistry Research:
2,1-Benzisoxazole,5-chloro-(7CI,8CI,9CI) is used as a research compound in medicinal chemistry. Its biological activity and potential therapeutic applications are being studied to explore its use in the treatment of various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 4596-92-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,9 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4596-92:
(6*4)+(5*5)+(4*9)+(3*6)+(2*9)+(1*2)=123
123 % 10 = 3
So 4596-92-3 is a valid CAS Registry Number.

4596-92-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Chloro-2,1-benzoxazole

1.2 Other means of identification

Product number -
Other names 5-CHLORO-2,1-BENZISOXAZOLE

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:4596-92-3 SDS

4596-92-3Upstream product

4596-92-3Relevant academic research and scientific papers

Reductive heterocyclizations via indium-iodine-promoted conversion of 2-nitroaryl imines or 2-nitroarenes to 2,3-diaryl-substituted indazoles

Ahn, Gil Hwan,Lee, Jung June,Jun, Young Moo,Lee, Byung Min,Kim, Byeong Hyo

, p. 2472 - 2485 (2008/02/13)

While N-(2-nitrobenzylidene)anilines produced mixtures of 2,1-benzisoxazoles and 3-anilino-2-aryl-2H-indazoles in the presence of indium and iodine in MeOH, N-(2-nitrobenzylidene)anilines were transformed into 3-anilino-2-aryl-2H-indazoles as the predominant major product through the change of the solvent from protic MeOH to aprotic THF. In an indium-mediated one-pot reductive reaction, 2-benzaldehydes and anilines in THF were also successfully transformed into the corresponding indazoles. This journal is The Royal Society of Chemistry.

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