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2101-86-2

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2101-86-2 Usage

Uses

4-Azidotoluene solution may be used for the functionalization at the axial position of boron subphthalocyanines with a terminal acetylene functionality via copper(I)-catalyzed azide-alkyne cycloaddition in the presence of Hunig′s base.

General Description

4-Azidotoluene is an aromatic azide generally used in copper(I)-catalyzed azide-alkyne cycloaddition reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 2101-86-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,0 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2101-86:
(6*2)+(5*1)+(4*0)+(3*1)+(2*8)+(1*6)=42
42 % 10 = 2
So 2101-86-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3/c1-6-2-4-7(5-3-6)9-10-8/h2-5H,1H3

2101-86-2 Well-known Company Product Price

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  • Aldrich

  • (727466)  4-Azidotoluenesolution  ~0.5 M in tert-butyl methyl ether, ≥95.0% (HPLC)

  • 2101-86-2

  • 727466-10ML

  • 1,627.47CNY

  • Detail
  • Aldrich

  • (727466)  4-Azidotoluenesolution  ~0.5 M in tert-butyl methyl ether, ≥95.0% (HPLC)

  • 2101-86-2

  • 727466-50ML

  • 6,165.90CNY

  • Detail

2101-86-2Relevant articles and documents

Cu(i)-catalyzed microwave-assisted synthesis of 1,2,3-triazole linked with 4-thiazolidinones: A one-pot sequential approach

Kumar, Yogesh,Matta, Akanksha,Kumar, Prashant,Parmar, Virinder S.,Van Der Eycken, Erik V.,Singh, Brajendra K.

, p. 1628 - 1639 (2015)

A novel copper(i) catalyzed, microwave-assisted one-pot, four-component sequential reaction between a propargyloxybenzaldehyde, a substituted phenyl azide, a substituted aniline and thioglycolic acid has been developed for the synthesis of 3-phenyl-2-[4-{

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Fischer,Anselme

, p. 5284 (1967)

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Spauschus,Scott

, p. 208 (1951)

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A mild TCEP-based para-azidobenzyl cleavage strategy to transform reversible cysteine thiol labelling reagents into irreversible conjugates

Maruani, Antoine,Alom, Shamim,Canavelli, Pierre,Lee, Maximillian T. W.,Morgan, Rachel E.,Chudasama, Vijay,Caddick, Stephen

, p. 5279 - 5282 (2015)

It has recently emerged that the succinimide linkage of a maleimide thiol addition product is fragile, which is a major issue in fields where thiol functionalisation needs to be robust. Herein we deliver a strategy that generates selective cysteine thiol

Triazole [5, 4-d] pyrimidone tricyclic compounds as well as preparation method and application thereof

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Paragraph 0064; 0067-0070; 0075, (2021/07/09)

The invention relates to triazole [5, 4-d] pyrimidone tricyclic compounds as well as a preparation method and application thereof.The triazole [5, 4-d] pyrimidone tricyclic compounds are prepared by following steps: taking different substituted anilines a

Selective CDK4/6 inhibition of novel 1,2,3-triazole tethered acridinedione derivatives induces G1/S cell cycle transition arrest via Rb phosphorylation blockade in breast cancer models

Praveenkumar,Gurrapu, Nirmala,Kolluri, Prashanth Kumar,Shivaraj,Subhashini,Dokala, Appaji

, (2021/10/12)

CDK4 & CDK6 are essential regulators of initial cell cycle phases and are always considered an exciting choice for anti-cancer therapy. In the present study, we presented the structure-based rational design & synthesis of a new class of 1,2,3-triazole tet

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