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3-Chloro-2-nitrobenzonitrile, a chemical compound with the molecular formula C7H3ClN2O2, is a yellow crystalline solid known for its role as a building block in the synthesis of pharmaceuticals, agrochemicals, and dyes. Its unique structure and properties make it a valuable intermediate in various chemical reactions.

34662-28-7

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34662-28-7 Usage

Uses

Used in Pharmaceutical Industry:
3-Chloro-2-nitrobenzonitrile is used as a key intermediate in the production of 2-aminopyridine, which is essential for the manufacturing of various pharmaceuticals. Its presence in the synthesis process contributes to the development of new and effective medications.
Used in Agrochemical Industry:
3-Chloro-2-nitrobenzonitrile is utilized as an intermediate in the synthesis of pesticides and herbicides. Its incorporation in these products helps enhance their effectiveness in controlling pests and weeds, thereby improving crop yields and quality.
Used in Dye Industry:
3-Chloro-2-nitrobenzonitrile serves as a building block in the creation of various dyes. Its chemical properties allow for the development of dyes with unique color characteristics and improved performance in different applications.
Safety Precautions:
Due to its hazardous nature, 3-Chloro-2-nitrobenzonitrile should be handled with care to avoid irritation to the skin, eyes, and respiratory system. Proper safety measures, such as wearing protective gear and working in well-ventilated areas, should be taken to minimize potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 34662-28-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,6 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 34662-28:
(7*3)+(6*4)+(5*6)+(4*6)+(3*2)+(2*2)+(1*8)=117
117 % 10 = 7
So 34662-28-7 is a valid CAS Registry Number.

34662-28-7SDS

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 3-chloro-2-nitrobenzonitrile

1.2 Other means of identification

Product number -
Other names nitrochlorobenzonitrile

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:34662-28-7 SDS

34662-28-7Relevant academic research and scientific papers

Synthesis and potent antifungal activity against Candida species of some novel 1H-benzimidazoles

Goeker, Hakan,Alp, Mehmet,Ates-Alagoez, Zeynep,Yildiz, Sulhiye

experimental part, p. 936 - 948 (2009/12/05)

(Chemical Equation Presented) A series of 47 novel N1-alkylated- 2-aryl-5(6)-substituted-1H-benzimidazoles and their three novel indole analogues were synthesized and evaluated for in vitro antifungal activities against Candida species by the tube dilution method. The results showed that compounds 79 and 80, having pyridine at the position C-2, of benzimidazoles exhibited the greatest activity with MIC values of 6.25-3.12 μg/mL. Indole analogues 108-110 have no inhibitory activity.

Use of EP4 receptor ligands in the treatment of IL-6 involved diseases

-

Page 116, (2010/02/06)

Methods of treating IL-6 involved diseases with EP4 receptor ligands, including EP4 receptor antagonists. Assays to determine the effect of test compounds on PGE2-induced whole blood cells activation.

EP4 RECEPTOR INHIBITORS TO TREAT RHEUMATOID ARTHRITIS

-

, (2008/06/13)

The invention features a method of treating rheumatoid arthritis in a mammal comprising administering an agent that inhibits prostaglandin EP4 receptor (EP4) activity. Also featured is a method of identifying agents that selectively inhibit EP4 activity in vivo.

Relaxation of smooth muscle in a mammal

-

, (2008/06/13)

4-Amino-6-arylpyrimidines and salts thereof, a novel class of inhibitors of platelet aggregation and broncho-dilators in mammals, and 4-hydroxy-6-arylpyrimidines as useful intermediates.

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