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2-Chloro-1-trityl-1H-imidazole is an imidazole derivative characterized by the presence of a chlorine atom at the 2nd position and a trityl group at the 1st position. It is a synthetic compound with a molecular structure that provides unique reactivity and stability, making it a versatile molecule for various applications in different industries.

67478-48-2

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67478-48-2 Usage

Uses

Used in Chemical Synthesis:
2-Chloro-1-trityl-1H-imidazole is used as a reagent in chemical synthesis for its ability to participate in reactions requiring an imidazole group. Its unique structure allows it to act as a catalyst or a building block in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Chloro-1-trityl-1H-imidazole is used as an intermediate in the synthesis of drug candidates. Its imidazole group can be incorporated into the molecular structure of potential therapeutic agents, providing specific biological activities and enhancing the drug's efficacy.
Used in Material Science:
2-Chloro-1-trityl-1H-imidazole can also be used in material science as a component in the development of new materials with unique properties. Its imidazole group can be utilized to create novel coordination complexes, which may have potential applications in areas such as sensors, catalysts, and advanced materials.
Used in Research and Development:
In research and development, 2-Chloro-1-trityl-1H-imidazole serves as a valuable tool for studying the properties and reactivity of imidazole-containing compounds. It can be used to investigate the mechanisms of various chemical reactions and to develop new synthetic methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 67478-48-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,4,7 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67478-48:
(7*6)+(6*7)+(5*4)+(4*7)+(3*8)+(2*4)+(1*8)=172
172 % 10 = 2
So 67478-48-2 is a valid CAS Registry Number.

67478-48-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Alfa Aesar

  • (H51861)  2-Chloro-1-tritylimidazole, 97%   

  • 67478-48-2

  • 250mg

  • 287.0CNY

  • Detail
  • Alfa Aesar

  • (H51861)  2-Chloro-1-tritylimidazole, 97%   

  • 67478-48-2

  • 1g

  • 1143.0CNY

  • Detail

67478-48-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-1-trityl-1H-imidazole

1.2 Other means of identification

Product number -
Other names 2-chloro-1-tritylimidazole

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:67478-48-2 SDS

67478-48-2Upstream product

67478-48-2Downstream Products

67478-48-2Relevant academic research and scientific papers

Zeolitic imidazolate frameworks for kinetic separation of propane and propene

Li, Kunhao,Olson, David H.,Seidel, Jonathan,Emge, Thomas J.,Gong, Hongwei,Zeng, Heping,Li, Jing

supporting information; experimental part, p. 10368 - 10369 (2009/12/06)

(Figure Presented) Propane/propene separation by cryogenic distillation is one of the most energy and cost intensive industrial processes. Adsorptive separation is a more energy-efficient alternative. Three isostructural zinc imidazolate zeolitic framewor

Synthesis of 2-aminoimidazole marine metabolites: clathrodine and 3'-amino-1'--prop-2'-ene

Daninos, Sophie,Mourabit, Ali Al,Ahond, Alain,Zurita, Manuel Bedoya,Poupat, Christiane,Potier, Pierre

, p. 590 - 599 (2007/10/02)

The synthesis of 2-aminoimidazole marine metabolites has induced various studies on the reactivity of the imidazole nucleus, especially in positions 2 and 4(5); these studies were helpful to prepare naturally occuring clathrodine and 3'-amino-1'-2-aminoi

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