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What is the (S)-amino(phenyl)acetonitrile ?
(S)-amino(phenyl)acetonitrile is , while it's Molecular Formula is C8H8N2.
What is the CAS number for (S)-amino(phenyl)acetonitrile ?
The CAS number of (S)-amino(phenyl)acetonitrile is 48108-77-6.
More information of (S)-amino(phenyl)acetonitrile 48108-77-6 are:
|
Synonyms |
L-phenylglycine nitrile;(S)-Amino-phenyl-acetonitrile; |
|
CAS?Number |
48108-77-6 |
|
Molecular Formula |
C8H8N2 |
|
Molecular Weight |
132.165 |
|
Density |
1.1g/cm3 |
|
Boiling Point |
235.8°Cat760mmHg |
|
Flash Point |
96.4°C |
|
PSA |
49.81000 |
|
LogP |
1.91028 |
What is (S)-amino(phenyl)acetonitrile (48108-77-6) used for?
(S)-amino(phenyl)acetonitrile, with the chemical formula C8H8N2, is an optically active compound featuring a chiral center. This characteristic allows it to exist in two enantiomeric forms, distinguishing it in various applications due to its specific spatial arrangement.
Usage:
Used in Pharmaceutical Industry:
(S)-amino(phenyl)acetonitrile is utilized as a fundamental building block in organic synthesis. Its primary application lies in the production of an array of drugs, capitalizing on its unique structural properties to create therapeutically beneficial compounds.
Used in Asymmetric Synthesis:
(S)-amino(phenyl)acetonitrile serves as a crucial reagent in asymmetric synthesis, a technique that allows for the creation of molecules with specific three-dimensional structures. This application is vital in producing enantiomerically pure compounds, which can have significantly different biological activities.
Used in Preparation of Chiral Molecules:
(S)-amino(phenyl)acetonitrile is also harnessed in the preparation of chiral molecules. Chirality is a critical factor in the efficacy and safety of pharmaceuticals, as different enantiomers of a drug can exhibit different pharmacological effects.
Used in Antitumor Applications:
Studies have revealed (S)-amino(phenyl)acetonitrile's potential as an antitumor agent. It is being investigated for its ability to interfere with cancer cell growth and proliferation, offering a promising avenue for the development of novel cancer treatments.
Used in Antimicrobial Applications:
Beyond its pharmaceutical applications, (S)-amino(phenyl)acetonitrile has also demonstrated antimicrobial properties. This suggests its potential use in the development of new antimicrobial agents to combat various infectious diseases.
InChI:InChI=1/C8H8N2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8H,10H2/t8-/m1/s1
Articles related to (S)-amino(phenyl)acetonitrile:
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Article |
Source |
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Process Optimisation Studies and Aminonitrile Substrate Evaluation of Rhodococcus erythropolis SET1, A Nitrile Hydrolyzing Bacterium |
Coady, Tracey M.,Coffey, Lee,Kinsella, Michael,Lennon, Claire M.,Mareya, Tatenda M.,O'Reilly, Catherine , p. 512 - 520 (2020/10/02) |
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The GAP chemistry for chiral N-phosphonyl imine-based Strecker reaction |
Kaur, Parminder,Wever, Walter,Pindi, Suresh,Milles, Raizada,Gu, Peng,Shi, Min,Li, Guigen scheme or table, p. 1288 - 1292 (2011/06/25) |
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