(S)-2-Amino-2-cyclohexylacetic acid hydrochloride

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Reagent Code: #38247
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CAS Number 191611-20-8

science Other reagents with same CAS 191611-20-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.67 g/mol
Formula C₈H₁₆ClNO₂
badge Registry Numbers
MDL Number MFCD00050539
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

(S)-2-Amino-2-cyclohexylacetic acid hydrochloride is primarily used in the pharmaceutical industry as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its enantiomeric purity makes it valuable in the development of drugs that require specific stereochemistry for efficacy, such as certain antiviral, antibacterial, and central nervous system (CNS) agents. Additionally, it serves as a key intermediate in the production of peptide-based therapeutics, where its structural properties contribute to the stability and biological activity of the final compounds. In research, it is utilized in the study of enzyme mechanisms and receptor interactions due to its ability to mimic natural amino acids in biochemical pathways.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿2,610.00
inventory 100g
10-20 days ฿5,112.00
inventory 5g
10-20 days ฿540.00
inventory 10g
10-20 days ฿1,062.00

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(S)-2-Amino-2-cyclohexylacetic acid hydrochloride
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(S)-2-Amino-2-cyclohexylacetic acid hydrochloride is primarily used in the pharmaceutical industry as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its enantiomeric purity makes it valuable in the development of drugs that require specific stereochemistry for efficacy, such as certain antiviral, antibacterial, and central nervous system (CNS) agents. Additionally, it serves as a key intermediate in the production of peptide-based therapeutics, where its st

(S)-2-Amino-2-cyclohexylacetic acid hydrochloride is primarily used in the pharmaceutical industry as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its enantiomeric purity makes it valuable in the development of drugs that require specific stereochemistry for efficacy, such as certain antiviral, antibacterial, and central nervous system (CNS) agents. Additionally, it serves as a key intermediate in the production of peptide-based therapeutics, where its structural properties contribute to the stability and biological activity of the final compounds. In research, it is utilized in the study of enzyme mechanisms and receptor interactions due to its ability to mimic natural amino acids in biochemical pathways.

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