328975-04-8
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Basic information
- Product Name: (2R)-3-allylsulfanyl-2-amino-propionic acid methyl ester
- Synonyms: (2R)-3-allylsulfanyl-2-amino-propionic acid methyl ester
- CAS NO:328975-04-8
- Molecular Formula:
- Molecular Weight: 175.252
- EINECS: N/A
- Product Categories: N/A
- Mol File: 328975-04-8.mol
- Article Data: 0
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (2R)-3-allylsulfanyl-2-amino-propionic acid methyl ester(CAS DataBase Reference)
- NIST Chemistry Reference: (2R)-3-allylsulfanyl-2-amino-propionic acid methyl ester(328975-04-8)
- EPA Substance Registry System: (2R)-3-allylsulfanyl-2-amino-propionic acid methyl ester(328975-04-8)
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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: 328975-04-8(Hazardous Substances Data)
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328975-04-8 Usage
Description
(2R)-3-allylsulfanyl-2-amino-propionic acid methyl ester is a chiral compound that is a methyl ester derivative of 3-allylsulfanyl-2-amino-propionic acid. It features a stereocenter at the second carbon atom and contains a thioether functional group (S-CH2-CH=CH2) along with an amino group. This molecule is frequently utilized in organic synthesis and medicinal chemistry due to its unique structure and reactivity.Uses
Used in Pharmaceutical Development:(2R)-3-allylsulfanyl-2-amino-propionic acid methyl ester is used as a key intermediate in the synthesis of pharmaceuticals for its potential role in drug design and discovery. Its unique structural features allow it to be a valuable component in the creation of new medicinal compounds.
Used in Organic Synthesis:
In the field of organic synthesis, (2R)-3-allylsulfanyl-2-amino-propionic acid methyl ester is used as a reactive building block for the assembly of more complex organic molecules. Its thioether and amino groups contribute to its versatility in various chemical reactions and transformations.
Used in Medicinal Chemistry:
(2R)-3-allylsulfanyl-2-amino-propionic acid methyl ester is utilized as a chiral auxiliary in medicinal chemistry to control the stereochemistry of target molecules. This is crucial for the development of enantiomerically pure drugs, as the stereochemistry of a compound can significantly affect its biological activity and safety profile.
Check Digit Verification of cas no
The CAS Registry Mumber 328975-04-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,8,9,7 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.Calculate Digit Verification of CAS Registry Number 328975-04:
(8*3)+(7*2)+(6*8)+(5*9)+(4*7)+(3*5)+(2*0)+(1*4)=178
178 % 10 = 8
So 328975-04-8 is a valid CAS Registry Number.
328975-04-8Upstream product
328975-04-8Downstream Products
- 857638-22-3 (2R)-3-allylsulfanyl-2-(2,4,6-trimethoxybenzylamino)-propionic acid methyl ester
- 556-27-4 Alliin
- 857638-40-5 (2R,2'S)-3-allylsulfanyl-2-[[2'-(9H-fluoren-9-ylmethoxycarbonylamino)-pent-4'-enoyl]-(2,4,6-trimethoxybenzyl)-amino]-propionic acid methyl ester
- 857638-37-0 (2R,2'S)-3-allylsulfanyl-2-{(2,4-dimethoxybenzyl)-[2'-(9H-fluoren-9-ylmethoxycarbonylamino)-pent-4'-enoyl]-amino}-propionic acid methyl ester
- 857638-21-2 (2R)-3-allylsulfanyl-2-(2,4-dimethoxybenzylamino)-propionic acid methyl ester
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(2R)-3-allylsulfanyl-2-amino-propionic acid methyl ester
