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(S)-α-methyl-3-iodophenylalanine is a chiral chemical compound derived from the amino acid phenylalanine. It is characterized by the presence of a methyl group and an iodine atom attached to the phenyl ring, which makes it a valuable tool for molecular labeling and imaging studies. (S)-α-methyl-3-iodophenylalanine is particularly notable for its (S)-enantiomer, which is the variant being referred to in this context. It serves as a precursor in the synthesis of various pharmaceuticals and biologically active molecules, with potential applications in medicinal chemistry, biochemistry, and neuropharmacology.

20846-40-6

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20846-40-6 Usage

Uses

Used in Pharmaceutical Synthesis:
(S)-α-methyl-3-iodophenylalanine is used as a precursor in the pharmaceutical industry for the synthesis of various biologically active molecules. Its unique structure allows for the creation of new drugs with potential therapeutic benefits.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-α-methyl-3-iodophenylalanine is used as a building block for designing and developing novel pharmaceuticals. Its chiral nature and functional groups make it a versatile compound for creating molecules with specific biological activities.
Used in Biochemistry:
(S)-α-methyl-3-iodophenylalanine is utilized in biochemistry for molecular labeling and imaging studies. (S)-α-methyl-3-iodophenylalanine's iodine atom can be employed for radiolabeling, which is essential for tracking and visualizing biological processes at the molecular level.
Used in Neuropharmacology:
In neuropharmacology, (S)-α-methyl-3-iodophenylalanine is used for the development of drugs targeting the central nervous system. Its structure may contribute to the creation of molecules that can modulate neurotransmission or affect neuronal function, potentially leading to treatments for neurological disorders.
Overall, (S)-α-methyl-3-iodophenylalanine is a versatile compound with a wide range of applications across different scientific disciplines, making it an important tool for research and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 20846-40-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,4 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20846-40:
(7*2)+(6*0)+(5*8)+(4*4)+(3*6)+(2*4)+(1*0)=96
96 % 10 = 6
So 20846-40-6 is a valid CAS Registry Number.

20846-40-6Downstream Products

20846-40-6Relevant academic research and scientific papers

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