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1-benzyl-4,5,6,7-tetrahydro-1H-benzo[d][1,2,3]triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15922-43-7

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15922-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15922-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,2 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15922-43:
(7*1)+(6*5)+(5*9)+(4*2)+(3*2)+(2*4)+(1*3)=107
107 % 10 = 7
So 15922-43-7 is a valid CAS Registry Number.

15922-43-7Downstream Products

15922-43-7Relevant academic research and scientific papers

One-Pot, Metal- And Azide-Free Synthesis of 1,2,3-Triazoles from α-Ketoacetals and Amines

Hawkins, Joel M.,Sutton, Scott C.,Zehnder, Luke R.

, p. 175 - 178 (2020)

An efficient one-pot two-step synthesis of 1,4-disubstituted 1,2,3-triazoles from α-ketoacetals and amines is presented. The method does not use metals, azides, or oxidants, and is compatible with a variety of functional groups, including heterocycles, esters, nitriles, and carbamates.

A Scalable Metal-, Azide-, and Halogen-Free Method for the Preparation of Triazoles

Clark, Peter R.,Hayes, Jerome F.,Tomkinson, Nicholas C. O.,Williams, Glynn D.

supporting information, p. 6740 - 6744 (2020/03/23)

A scalable metal-, azide-, and halogen-free method for the synthesis of substituted 1,2,3-triazoles has been developed. The reaction proceeds through a 3-component coupling of α-ketoacetals, tosyl hydrazide, and a primary amine. The reaction shows outstanding functional-group tolerance with respect to both the α-ketoacetal and amine coupling partners, providing access to 4-, 1,4-, 1,5-, and 1,4,5-substituted triazoles in excellent yield. This robust method results in densely functionalised 1,2,3-triazoles that remain challenging to prepare by azide–alkyne cycloaddition (AAC, CuAAC, RuAAC) methods and can be scaled in either batch or flow reactors. Methods for the chemoselective reaction of either aliphatic amines or anilines are also described, revealing some of the potential of this novel and highly versatile transformation.

Generation of cycloheptynes and cyclooctynes via a sulfoxide-magnesium exchange reaction of readily synthesized 2-sulfinylcycloalkenyl triflates

Yoshida, Suguru,Karaki, Fumika,Uchida, Keisuke,Hosoya, Takamitsu

, p. 8745 - 8748 (2015/05/20)

Cycloheptynes and cyclooctynes were efficiently generated via a sulfoxide-magnesium exchange reaction of readily synthesized 2-sulfinylcycloalkenyl triflates. Cycloadditions between various ynophiles and the cycloalkynes generated by this method proceeded

Cycloadditions of cyclohexynes and cyclopentyne

Medina, Jose M.,McMahon, Travis C.,Jimnez-Oss, Gonzalo,Houk,Garg, Neil K.

supporting information, p. 14706 - 14709 (2014/12/11)

We report the strategic use of cyclohexyne and the more elusive intermediate, cyclopentyne, as a tool for the synthesis of new heterocyclic compounds. Experimental and computational studies of a 3-substituted cyclohexyne are also described. The observed regioselectivities are explained by the distortion/interaction model.

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