1H-Indole-2-propanoic acid, α-amino, (αS)-, also known as L-Tryptophan, is an essential amino acid that plays a crucial role in various biological processes. It is a naturally occurring compound with a molecular formula of C11H12N2O2 and a molecular weight of 204.23 g/mol. L-Tryptophan is characterized by its indole ring and a propanoic acid side chain, which is attached to the α-amino group. This amino acid is synthesized in plants and microorganisms but cannot be produced by the human body, making it a dietary essential. It is involved in the biosynthesis of proteins, serotonin production, and niacin (vitamin B3) formation. L-Tryptophan is found in various foods, including meat, fish, dairy products, and legumes, and is also available as a dietary supplement.
533-42-6
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Basic information
- Product Name: 1H-Indole-2-propanoic acid, .alpha.-amino-, (.alpha.S)-
- Synonyms: 1H-Indole-2-propanoic acid, .alpha.-amino-, (.alpha.S)-
- CAS NO:533-42-6
- Molecular Formula: C11H12N2O2
- Molecular Weight: 204.23
- EINECS: N/A
- Product Categories: N/A
- Mol File: 533-42-6.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 1H-Indole-2-propanoic acid, .alpha.-amino-, (.alpha.S)-(CAS DataBase Reference)
- NIST Chemistry Reference: 1H-Indole-2-propanoic acid, .alpha.-amino-, (.alpha.S)-(533-42-6)
- EPA Substance Registry System: 1H-Indole-2-propanoic acid, .alpha.-amino-, (.alpha.S)-(533-42-6)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 533-42-6(Hazardous Substances Data)
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1H-Indole-2-propanoic acid
an amino acid belonging to the category of indole derivativesChiral molecule
has a non-superimposable mirror image(αS)-enantiomer
the biologically active form of the moleculeIntermediate in the biosynthesis of the plant hormone auxin
regulates various aspects of plant growth and developmentPotential pharmacological properties
studied for its anti-inflammatory and anti-cancer effectsUsed in research and as a starting material for the synthesis of other indole derivatives with potential therapeutic applications
Promise in both the agricultural and medical fields
due to its diverse biological activities.Check Digit Verification of cas no
The CAS Registry Mumber 533-42-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.Calculate Digit Verification of CAS Registry Number 533-42:
(5*5)+(4*3)+(3*3)+(2*4)+(1*2)=56
56 % 10 = 6
So 533-42-6 is a valid CAS Registry Number.
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1H-Indole-2-propanoic acid, .alpha.-amino-, (.alpha.S)-
