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53366-30-6

2-(isoquinolin-4-yl)acetic acid hydrochloride

Catalog#: AR01B680  |   CAS#: 53366-30-6  |   MDL#: MFCD30181104  |   MF: C11H10ClNO2  |   MW: 223.6556

Packsize Purity Price Availability Quantity
50mg 95% $307.00 2-3 weeks Buy Now Add To Cart
100mg 95% $446.00 2-3 weeks Buy Now Add To Cart
250mg 95% $628.00 2-3 weeks Buy Now Add To Cart
500mg 95% $976.00 2-3 weeks Buy Now Add To Cart
1g 95% $1,241.00 2-3 weeks Buy Now Add To Cart
2.5g 95% $2,411.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR01B680
Chemical Name 2-(isoquinolin-4-yl)acetic acid hydrochloride
CAS Number 53366-30-6
Molecular Formula C11H10ClNO2
Molecular Weight 223.6556
MDL Number MFCD30181104
SMILES OC(=O)Cc1cncc2c1cccc2.Cl

2-(Isoquinolin-4-yl)acetic acid hydrochloride, also known as $name$, is a versatile compound widely used in chemical synthesis. In organic chemistry, this compound serves as a key building block for the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure containing an isoquinoline ring confers specific reactivity and functionality that make it valuable in synthetic routes.One common application of 2-(Isoquinolin-4-yl)acetic acid hydrochloride is as a precursor for the synthesis of heterocyclic compounds with potential biological activities. By leveraging the reactivity of the isoquinoline moiety, researchers can introduce diverse functional groups and modify the structure to fine-tune the properties of the final product. This versatility allows for the creation of new drug candidates, bioactive molecules, and materials with tailored characteristics.Additionally, 2-(Isoquinolin-4-yl)acetic acid hydrochloride can be utilized in the preparation of ligands for metal-catalyzed reactions, asymmetric synthesis, and other advanced synthetic methodologies. Its presence in the molecular structure can influence the stereochemistry and regiochemistry of the reactions, leading to controlled outcomes and improved selectivity. This compound acts as a valuable tool for chemists seeking to design efficient and precise synthetic routes for complex molecules.In summary, the application of 2-(Isoquinolin-4-yl)acetic acid hydrochloride in chemical synthesis extends to the construction of diverse organic compounds, enabling the development of novel materials, pharmaceuticals, and chemical entities with tailored properties and functionalities.
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GHS Pictogram N/A
UN# -
Hazard Statements -
Class -
Packing Group -

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