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77792-52-0

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77792-52-0 Usage

Structure

A derivative of benzisoxazole, a heterocyclic compound with a benzene ring fused to an oxazole ring.

Chlorine content

The presence of chloro and chlorophenyl groups in its structure.

Potential applications

Pharmaceutical, agrochemical, and material science industries.

Importance

An important building block for the synthesis of various biologically active compounds and as a key intermediate in the development of new drugs and materials.

Pharmacological properties

May exhibit certain pharmacological properties which could make it an important target for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 77792-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,7,9 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77792-52:
(7*7)+(6*7)+(5*7)+(4*9)+(3*2)+(2*5)+(1*2)=180
180 % 10 = 0
So 77792-52-0 is a valid CAS Registry Number.

77792-52-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-3-(2-chlorophenyl)-2,1-benzisoxazole

1.2 Other means of identification

Product number -
Other names 5-Chloro-3-(2-chlorophenyl)benzo[c]isoxazole

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:77792-52-0 SDS

77792-52-0Relevant articles and documents

Metal-Free Synthesis of Anthranils by PhIO Mediated Heterocyclization of ortho-Carbonyl Anilines

Garia, Alankrita,Grover, Jatin,Jain, Nidhi

, p. 4125 - 4131 (2021/08/24)

Here, we report a metal-free synthesis of anthranils from ortho-carbonyl anilines using PhIO as a sole additive under ambient conditions. This methodology did not require any external additives and delivered anthranils in excellent yields with broad substrate scope. The mechanistic studies suggest that the reaction proceeds via in-situ generation of iminoiodane leading to nitrene and a subsequent nucleophilic attack from oxygen of ortho-carbonyl aniline on nitrene results in heterocyclization.

Psychotropic derivatives of 5-phenyl-7-chloro-1,3-dihydro-1,4-benzodiazepin-2-one and contribution to the synthesis of its 5-(2-chlorophenyl) analogue

Vejdelek,Rajsner,Dlabac,et al.

, p. 3593 - 3615 (2007/10/02)

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