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1003310-07-3

2-(1-Benzyl-1H-1,2,3-triazol-4-yl)acetic acid is a versatile chemical compound featuring a central triazole ring with a benzyl group and an acetic acid group attached to it. 2-(1-Benzyl-1H-1,2,3-triazol-4-yl)acetic acid is widely recognized for its potential in organic synthesis and medicinal chemistry, serving as a valuable building block for the creation of various biologically active compounds. The triazole ring's ability to bind to biological targets, combined with the benzyl group's capacity for structural manipulation and the acetic acid group's potential for further functionalization, make this molecule a promising intermediate in drug discovery and development.

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  • 1003310-07-3 Structure

  • Basic information

    1. Product Name: 2-(1-Benzyl-1H-1,2,3-triazol-4-yl)acetic acid
    2. Synonyms: 2-(1-Benzyl-1H-1,2,3-triazol-4-yl)acetic acid;(1-Benzyl-1H-1,2,3-triazol-4-yl)acetic acid
    3. CAS NO:1003310-07-3
    4. Molecular Formula: C11H11N3O2
    5. Molecular Weight: 217.22394
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1003310-07-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(1-Benzyl-1H-1,2,3-triazol-4-yl)acetic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(1-Benzyl-1H-1,2,3-triazol-4-yl)acetic acid(1003310-07-3)
    11. EPA Substance Registry System: 2-(1-Benzyl-1H-1,2,3-triazol-4-yl)acetic acid(1003310-07-3)

  • 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: 1003310-07-3(Hazardous Substances Data)

1003310-07-3 Usage

Uses

Used in Organic Synthesis:
2-(1-Benzyl-1H-1,2,3-triazol-4-yl)acetic acid is used as a building block for the synthesis of a variety of compounds due to its structural features that facilitate easy manipulation and functionalization.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-(1-Benzyl-1H-1,2,3-triazol-4-yl)acetic acid is utilized as a key intermediate for the development of biologically active molecules, capitalizing on the triazole ring's affinity for binding to biological targets, which is crucial for drug efficacy.
Used in Drug Development:
2-(1-Benzyl-1H-1,2,3-triazol-4-yl)acetic acid is employed as a starting material in drug development, leveraging its versatile structure to create compounds with potential therapeutic applications, particularly in the discovery of new pharmaceuticals.
Used in Pharmaceutical Industry:
Within the pharmaceutical industry, 2-(1-Benzyl-1H-1,2,3-triazol-4-yl)acetic acid is used as a precursor in the synthesis of drug candidates, taking advantage of its chemical properties to enhance the potency, selectivity, and pharmacokinetic properties of new medications.

Check Digit Verification of cas no

The CAS Registry Mumber 1003310-07-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,3,3,1 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1003310-07:
(9*1)+(8*0)+(7*0)+(6*3)+(5*3)+(4*1)+(3*0)+(2*0)+(1*7)=53
53 % 10 = 3
So 1003310-07-3 is a valid CAS Registry Number.

1003310-07-3Downstream Products

1003310-07-3Relevant articles and documents

Redox-Robust Pentamethylferrocene Polymers and Supramolecular Polymers, and Controlled Self-Assembly of Pentamethylferricenium Polymer-Embedded Ag, AgI, and Au Nanoparticles

Gu, Haibin,Ciganda, Roberto,Castel, Patricia,Vax, Amélie,Gregurec, Danijela,Irigoyen, Joseba,Moya, Sergio,Salmon, Lionel,Zhao, Pengxiang,Ruiz, Jaime,Hernández, Ricardo,Astruc, Didier

, p. 18177 - 18186 (2015)

We report the first pentamethylferrocene (PMF) polymers and the redox chemistry of their robust polycationic pentamethylferricenium (PMFium) analogues. The PMF polymers were synthesized by ring-opening metathesis polymerization (ROMP) of a PMF-containing

Cu(I)-catalyzed intramolecular cyclization of alkynoic acids in aqueous media: A "click side reaction"

Mindt, Thomas L.,Schibli, Roger

, p. 10247 - 10250 (2008/03/28)

(Chemical Equation Presented) Alkynoic acids, in particular, 4-pentynoic acid derivatives, undergo intramolecular cyclizations to enol lactones under reaction conditions typically applied for the Cu(I)-catalyzed cycloaddition of terminal alkynes and azide

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