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4600-03-7

1-Phenyl-4-(propan-1-ol-3-yl)-1H-1,2,3-triazole is a complex organic compound with the molecular formula C12H14N2O. It is a derivative of 1,2,3-triazole, a five-membered heterocyclic ring containing three nitrogen atoms. The structure of 1-phenyl-4-(propan-1-ol-3-yl)-1H-1,2,3-triazole features a phenyl group (C6H5) attached to the 1-position of the triazole ring, and a propan-1-ol-3-yl group (C3H7OH) attached to the 4-position. 1-phenyl-4-(propan-1-ol-3-yl)-1H-1,2,3-triazole is of interest in various chemical and pharmaceutical applications due to its unique structure and potential reactivity. It is important to note that the specific properties, applications, and safety considerations of 1-phenyl-4-(propan-1-ol-3-yl)-1H-1,2,3-triazole should be evaluated through detailed studies and in accordance with relevant chemical regulations.

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  • 4600-03-7 Structure

  • Basic information

    1. Product Name: 1-phenyl-4-(propan-1-ol-3-yl)-1H-1,2,3-triazole
    2. Synonyms: 1-phenyl-4-(propan-1-ol-3-yl)-1H-1,2,3-triazole
    3. CAS NO:4600-03-7
    4. Molecular Formula:
    5. Molecular Weight: 203.244
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 4600-03-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-phenyl-4-(propan-1-ol-3-yl)-1H-1,2,3-triazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-phenyl-4-(propan-1-ol-3-yl)-1H-1,2,3-triazole(4600-03-7)
    11. EPA Substance Registry System: 1-phenyl-4-(propan-1-ol-3-yl)-1H-1,2,3-triazole(4600-03-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 4600-03-7(Hazardous Substances Data)

4600-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4600-03-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,0 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4600-03:
(6*4)+(5*6)+(4*0)+(3*0)+(2*0)+(1*3)=57
57 % 10 = 7
So 4600-03-7 is a valid CAS Registry Number.

4600-03-7Downstream Products

4600-03-7Relevant articles and documents

A one-pot, copper-catalyzed azidation/click reaction of aryl and heteroaryl bromides in an environmentally friendly deep eutectic solvent

Kafle, Arjun,Handy, Scott T.

, p. 7024 - 7029 (2017)

In an effort to avoid the hazards of isolating and handling azides in click chemistry, many groups have turned to in situ generation of azides from halide precursors. This option is readily accomplished for alkyl azides, but is more challenging for aryl a

Application of two magnetic nanoparticle-supported copper(I) catalysts for the synthesis of triazole derivatives

Mohammadi, Leila,Zolifgol, Mohammad Ali,Yarie, Meysam,Ebrahiminia, Mahsa,Roberts, Kenneth P.,Hussaini, Syed R.

, p. 4789 - 4799 (2019/06/11)

Catalytic performance of two magnetically recoverable copper(I) complexes is reported for the synthesis of 1,2,3-triazole derivatives. Boronic acids and alkyl halides, in the presence of either catalyst, react with terminal alkynes and NaN3, fo

Pressure-accelerated azide-alkyne cycloaddition: Micro capillary versus autoclave reactor performance

Borukhova, Svetlana,Seeger, Andreas D.,Nol, Timothy,Wang, Qi,Busch, Markus,Hessel, Volker

, p. 504 - 512 (2015/03/04)

Pressure effects on regioselectivity and yield of cycloaddition reactions have been shown to exist. Nevertheless, high pressure synthetic applications with subsequent benefits in the production of natural products are limited by the general availability o

Microwave enhancement of a 'one-pot' tandem azidation-'click' cycloaddition of anilines

Moorhouse, Adam D.,Moses, John E.

scheme or table, p. 2089 - 2092 (2009/04/07)

The practical and efficient one-pot azidation of anilines with the reagent combination t-BuONO and TMSN3 has become a useful addition to the click-chemistry toolbox. Herein we report a modification of this methodology, using microwave radiation

One-pot synthesis of 1,4-disubstituted 1,2,3-triazoles from in situ generated azides

Feldman, Alina K.,Colasson, Benoit,Fokin, Valery V.

, p. 3897 - 3899 (2007/10/03)

(Chemical Equation Presented) 1,4-Disubstituted 1,2,3-triazoles are obtained in excellent yields by a convenient one-pot procedure from a variety of readily available aromatic and aliphatic halides without isolation of potentially unstable organic azide intermediates.

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