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BOC-(S)-3-amino-3-(3-fluoro-phenyl)-propionic acid is a chiral amino acid derivative with the molecular formula C14H18FNO4. It features a BOC (tert-butoxycarbonyl) protecting group on the amino group and a stereocenter at the alpha carbon, which gives it an S configuration. BOC-(S)-3-AMINO-3-(3-FLUORO-PHENYL)-PROPIONIC ACID is commonly utilized in organic synthesis and medicinal chemistry as a key building block for the development of peptide and protein-based drugs. The incorporation of a fluorine atom in the phenyl ring may confer unique biological and pharmacological properties, making BOC-(S)-3-amino-3-(3-fluoro-phenyl)-propionic acid a significant chemical in the creation of pharmaceuticals and biologically active molecules.

500770-72-9

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500770-72-9 Usage

Uses

Used in Pharmaceutical Industry:
BOC-(S)-3-amino-3-(3-fluoro-phenyl)-propionic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into the structure of peptide and protein-based drugs. The presence of the fluorine atom in the phenyl ring may enhance the compound's pharmacological properties, such as increasing lipophilicity, metabolic stability, and receptor binding affinity.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, BOC-(S)-3-amino-3-(3-fluoro-phenyl)-propionic acid serves as a valuable building block for the design and synthesis of novel bioactive compounds. Its unique structural features, including the BOC protecting group and the S configuration, allow for the exploration of new chemical space and the development of potential therapeutic agents with improved efficacy and selectivity.
Used in Organic Synthesis:
BOC-(S)-3-amino-3-(3-fluoro-phenyl)-propionic acid is employed as a versatile synthetic building block in organic synthesis. Its reactivity and functional group compatibility make it suitable for various synthetic transformations, enabling the preparation of a wide range of chemical compounds with diverse applications in materials science, agrochemicals, and other specialty chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 500770-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,7,7 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 500770-72:
(8*5)+(7*0)+(6*0)+(5*7)+(4*7)+(3*0)+(2*7)+(1*2)=119
119 % 10 = 9
So 500770-72-9 is a valid CAS Registry Number.

500770-72-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-3-((tert-Butoxycarbonyl)amino)-3-(3-fluorophenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names (3S)-3-(3-fluorophenyl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:500770-72-9 SDS

500770-72-9Relevant academic research and scientific papers

N-4-PIPERIDINYL COMPOUNDS AS CCR5 MODULATORS

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, (2010/02/05)

The invention provides a compound of formula (I):[Chemical formula should be inserted here. Please see paper copy.] wherein R1, R2, R3, R3a, R4, R4a, R5, and R6 are as defined; or a pharmaceutically acceptable salt thereof or a solvate thereof; compositions containing these compounds, processes for preparing them and their use as modulators of chemokine activity (especially CCR5 activity).

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