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4-METHYL-2-NITROPHENYL ISOTHIOCYANATE, with the molecular formula C8H6N2O2S, is a yellow solid chemical compound. It is widely utilized in organic synthesis as a reagent for incorporating the isothiocyanate functional group into organic molecules. Known for its strong pungent odor, 4-METHYL-2-NITROPHENYL ISOTHIOCYANATE is also recognized as an irritant to the skin, eyes, and respiratory system, necessitating careful handling and the use of appropriate personal protective equipment.

17614-74-3

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17614-74-3 Usage

Uses

Used in Organic Synthesis:
4-METHYL-2-NITROPHENYL ISOTHIOCYANATE is used as a reagent for the introduction of the isothiocyanate functional group into organic molecules. This application is crucial for the synthesis of various organic compounds, as the isothiocyanate group can be further reacted or serve as a key intermediate in the formation of complex organic structures.
Used in Chemical Research:
In the field of chemical research, 4-METHYL-2-NITROPHENYL ISOTHIOCYANATE is employed as a tool to study the reactivity and properties of the isothiocyanate functional group. This helps in understanding the underlying mechanisms of reactions involving isothiocyanates and contributes to the development of new synthetic methodologies and applications.
Used in Pharmaceutical Industry:
4-METHYL-2-NITROPHENYL ISOTHIOCYANATE is used as a building block in the synthesis of pharmaceutical compounds. The isothiocyanate group can be incorporated into drug molecules to enhance their biological activity or to create new drugs with unique therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 4-METHYL-2-NITROPHENYL ISOTHIOCYANATE is utilized in the development of pesticides and other agrochemicals. The isothiocyanate group can be used to create new active ingredients with improved efficacy and selectivity against pests and diseases.
Used in Material Science:
4-METHYL-2-NITROPHENYL ISOTHIOCYANATE is employed in the synthesis of materials with specific properties, such as polymers, coatings, and adhesives. The isothiocyanate group can be used to create cross-linking or grafting reactions, leading to materials with enhanced mechanical, thermal, or chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 17614-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,1 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17614-74:
(7*1)+(6*7)+(5*6)+(4*1)+(3*4)+(2*7)+(1*4)=113
113 % 10 = 3
So 17614-74-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O2S/c1-6-2-3-7(9-5-13)8(4-6)10(11)12/h2-4H,1H3

17614-74-3 Well-known Company Product Price

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  • Alfa Aesar

  • (L10438)  4-Methyl-2-nitrophenyl isothiocyanate, 95%   

  • 17614-74-3

  • 1g

  • 331.0CNY

  • Detail
  • Alfa Aesar

  • (L10438)  4-Methyl-2-nitrophenyl isothiocyanate, 95%   

  • 17614-74-3

  • 5g

  • 1497.0CNY

  • Detail

17614-74-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-METHYL-2-NITROPHENYL ISOTHIOCYANATE

1.2 Other means of identification

Product number -
Other names 4-Methyl-2-nitrophenyl isothiocyanate

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:17614-74-3 SDS

17614-74-3Relevant academic research and scientific papers

Synthesis of 2-Arylaminobenzothiazoles and Aryl Isothiocyanates as Antitubercular Agents

Pande, Anil,Lokhande, S. R.,Patel, Madhuben R.,Khadse, B. G.

, p. 311 - 312 (2007/10/02)

A series of 2-arylaminobenzothiazoles (II) and aryl isothiocyanates (I) bearing a nitro group in the aryl moiety have been synthesized and screened against M. tuberculosis (H37Rv) in vitro.Most of the isothiocyanate derivatives (I) show antitub

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