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175789-75-0

1-methyl-5-phenyl-1H-1,2,3-triazole-4-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 175789-75-0 Structure

  • Basic information

    1. Product Name: 1-methyl-5-phenyl-1H-1,2,3-triazole-4-carbonitrile
    2. Synonyms: 1-methyl-5-phenyl-1H-1,2,3-triazole-4-carbonitrile
    3. CAS NO:175789-75-0
    4. Molecular Formula:
    5. Molecular Weight: 184.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 175789-75-0.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-methyl-5-phenyl-1H-1,2,3-triazole-4-carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-methyl-5-phenyl-1H-1,2,3-triazole-4-carbonitrile(175789-75-0)
    11. EPA Substance Registry System: 1-methyl-5-phenyl-1H-1,2,3-triazole-4-carbonitrile(175789-75-0)

  • 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: 175789-75-0(Hazardous Substances Data)

175789-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 175789-75-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,7,8 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 175789-75:
(8*1)+(7*7)+(6*5)+(5*7)+(4*8)+(3*9)+(2*7)+(1*5)=200
200 % 10 = 0
So 175789-75-0 is a valid CAS Registry Number.

175789-75-0Relevant articles and documents

One-pot, three-component synthesis of 1,4,5-trisubstituted 1,2,3-triazoles starting from primary alcohols

Jin, Guanyi,Zhang, Jian,Fu, Dan,Wu, Jingjing,Cao, Song

supporting information, p. 5446 - 5449 (2012/10/30)

A novel, one-pot, three-component approach for the synthesis of 1,4,5-trisubstituted 1,2,3-triazoles through the cycloaddition of a wide range of primary alcohols with sodium azide and active methylene ketones in the presence of N-(p-toluenesulfonyl)imidazole, tetrabutylammonium iodide, and triethylamine in DMF/DMSO has been developed.

REACTION DU METHYLAZIDE AVEC DES OLEFINES CINNAMIQUES, CROTONIQUES ET ACRYLIQUES. ETUDE DES COMPOSES OBTENUS

Hetet, G. Le,Benhaoua, H.,Carrie, R.

, p. 189 - 204 (2007/10/03)

Methylazide reacts with the title olefines and gives expected 1,2,3-triazolines in equilibrium with corresponding amino dizao compounds.Because this equilibrium, E and Z olefines gives the same result, and the addition do not seem stereospecific.Thermolys

REACTIONS DES METHYLAZIDE ET PHENYLAZIDE AVEC QUELQUES ALCYNES ET OLEFINES α-NITREES. SYNTHESE REGIOSPECIFIQUE DES 1,2,3 TRIAZOLES

Piet, J. C.,Hetet, G. Le,Cailleux, P.,Benhaoua, H.,Carrie, R.

, p. 33 - 44 (2007/10/03)

The reactions of alkynes and α-nitro-olefines with methylazide and phenylazide was studied.In contrast to known reactions with alkynes which are non-regioselective, methylazide and phenylazide react regiospecifically with α-nitro-olefines and give only one type of triazole after elimination of HNO2.These reactions are very useful synthetic approaches to 1,2,3 triazoles.

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