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2-CHLORO-4-NITROPHENYL ISOCYANATE is a chemical compound characterized by its molecular formula C7H3ClN2O3. It is a yellow crystalline solid known for its high reactivity and is primarily utilized in the synthesis of pharmaceuticals, agrochemicals, and dyes. As an isocyanate, it is a key component in the production of polyurethane polymers. Due to its potential to cause irritation and act as an allergen and sensitizer, it requires careful handling and proper safety measures.

40397-95-3

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40397-95-3 Usage

Uses

Used in Pharmaceutical Industry:
2-CHLORO-4-NITROPHENYL ISOCYANATE is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its reactivity allows for the creation of new drug molecules with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-CHLORO-4-NITROPHENYL ISOCYANATE is employed as a precursor in the development of pesticides and other agrochemical products, contributing to the production of effective solutions for crop protection.
Used in Dye Industry:
2-CHLORO-4-NITROPHENYL ISOCYANATE is utilized as a building block in the formulation of dyes, providing a range of color options for various applications, including textiles and other industrial processes.
Used in Polymer Industry:
As an isocyanate, 2-CHLORO-4-NITROPHENYL ISOCYANATE is used in the production of polyurethane polymers, which are versatile materials with applications in coatings, adhesives, and flexible foams.
Safety Precautions:
Due to its potential to cause irritation to the skin, eyes, and respiratory system, as well as its allergenic and sensitizing properties, 2-CHLORO-4-NITROPHENYL ISOCYANATE requires proper handling and safety measures. Workers should use appropriate personal protective equipment and follow established safety protocols when working with this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 40397-95-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,9 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40397-95:
(7*4)+(6*0)+(5*3)+(4*9)+(3*7)+(2*9)+(1*5)=123
123 % 10 = 3
So 40397-95-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H3ClN2O3/c8-6-3-5(10(12)13)1-2-7(6)9-4-11/h1-3H

40397-95-3 Well-known Company Product Price

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  • Alfa Aesar

  • (L12685)  2-Chloro-4-nitrophenyl isocyanate, 97%   

  • 40397-95-3

  • 1g

  • 271.0CNY

  • Detail
  • Alfa Aesar

  • (L12685)  2-Chloro-4-nitrophenyl isocyanate, 97%   

  • 40397-95-3

  • 5g

  • 902.0CNY

  • Detail
  • Aldrich

  • (478369)  2-Chloro-4-nitrophenylisocyanate  99%

  • 40397-95-3

  • 478369-1G

  • 288.99CNY

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40397-95-3SDS

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 2-CHLORO-4-NITROPHENYL ISOCYANATE

1.2 Other means of identification

Product number -
Other names 2-Chloro-4-nitrophenyl isocyanate

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:40397-95-3 SDS

40397-95-3Relevant academic research and scientific papers

Design, synthesis and antitumor activity of 4-aminoquinazoline derivatives targeting VEGFR-2 tyrosine kinase

Yu, Bing,Tang, Li-Da,Li, Yi-Liang,Song, Shu-Hui,Ji, Xiao-Liang,Lin, Mu-Sen,Wu, Chun-Fu

scheme or table, p. 110 - 114 (2012/02/16)

We report herein the design and synthesis of novel 4-aminoquinazoline derivatives based on the inhibitors of VEGFR-2 tyrosine kinases. The VEGFR-2 inhibitory activities of these newly synthesized compounds were also evaluated and compared with that of ZD6

Novel and efficient synthesis of 4-substituted-1,2,4-triazolidine-3,5- diones from anilines

Mallakpour, Shadpour,Rafiee, Zahra

, p. 1927 - 1934 (2008/02/04)

A simple and efficient three-step synthetic procedure for the preparation of 4-substituted phenyl derivatives of 1,2,4-triazolidindiones (urazoles), starting from anilines, has been developed. In this method, aniline derivatives were reacted with 4-nitrophenyl chloroformate to provide corresponding carbamate derivatives. In the second step, semicarbazide derivatives were prepared from these carbamates by reaction with ethyl carbazate. The cyclization reaction of corresponding semicarbazides furnished 1,2,4-triazolidindiones in high yields. Copyright Taylor & Francis Group, LLC.

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