(R)-tert-Butyl (1-aminopropan-2-yl)carbamate hydrochloride

95%

Reagent Code: #37276
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CAS Number 1217631-35-0

science Other reagents with same CAS 1217631-35-0

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Weight 210.7000 g/mol
Formula C₈H₁₉ClN₂O₂
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MDL Number MFCD11109482
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description Product Description

This compound is primarily used in the synthesis of chiral intermediates for pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require specific stereochemistry. It serves as a key building block in the production of drugs targeting neurological disorders, cardiovascular diseases, and certain types of cancer. Its chiral nature ensures the desired biological activity and efficacy of the final drug product. Additionally, it is employed in peptide synthesis and as a protecting group for amines in organic chemistry, facilitating complex molecular constructions. Its hydrochloride form enhances stability and solubility, making it suitable for various chemical reactions and formulations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,990.00
inventory 1g
10-20 days ฿8,660.00
inventory 5g
10-20 days ฿36,180.00

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(R)-tert-Butyl (1-aminopropan-2-yl)carbamate hydrochloride
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This compound is primarily used in the synthesis of chiral intermediates for pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require specific stereochemistry. It serves as a key building block in the production of drugs targeting neurological disorders, cardiovascular diseases, and certain types of cancer. Its chiral nature ensures the desired biological activity and efficacy of the final drug product. Additionally, it is employed in peptide synthesis and

This compound is primarily used in the synthesis of chiral intermediates for pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require specific stereochemistry. It serves as a key building block in the production of drugs targeting neurological disorders, cardiovascular diseases, and certain types of cancer. Its chiral nature ensures the desired biological activity and efficacy of the final drug product. Additionally, it is employed in peptide synthesis and as a protecting group for amines in organic chemistry, facilitating complex molecular constructions. Its hydrochloride form enhances stability and solubility, making it suitable for various chemical reactions and formulations.

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