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BOC-(S)-3-AMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID is a chemical compound with the molecular formula C14H19NO5, characterized by its unique structural features including a BOC (tert-butoxycarbonyl) protecting group. This derivative of 3-amino-3-(3-hydroxy-phenyl)-propionic acid is utilized as a versatile building block in the realms of organic synthesis and pharmaceutical research. The BOC protecting group allows for mild acidic deprotection, revealing the free amine group for subsequent chemical reactions, thereby enhancing its utility in the creation of new drugs and bioactive molecules.

499995-79-8

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499995-79-8 Usage

Uses

Used in Pharmaceutical Research:
BOC-(S)-3-AMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID is used as a key intermediate in the synthesis of various pharmaceutical compounds due to its ability to be selectively deprotected and functionalized. The presence of the BOC group facilitates the protection of the amine during the synthesis process, ensuring the integrity of the molecule and allowing for the development of complex drug structures.
Used in Organic Synthesis:
In the field of organic synthesis, BOC-(S)-3-AMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID is employed as a versatile building block for the creation of a wide range of organic molecules. Its unique structure and the presence of the BOC protecting group make it a valuable component in the synthesis of complex organic compounds, including those with potential applications in material science, agrochemicals, and specialty chemicals.
Used in Drug Development:
BOC-(S)-3-AMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID is utilized as a precursor in the development of new drugs and bioactive molecules. Its unique structural features and the ability to selectively remove the BOC protecting group under mild acidic conditions make it an attractive candidate for the design and synthesis of novel therapeutic agents with potential applications in various medical fields.
Used in Bioactive Molecule Design:
BOC-(S)-3-AMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID is also used as a structural component in the design of bioactive molecules, where its specific functional groups and the BOC protecting group can be leveraged to create molecules with targeted biological activities. The potential applications of these bioactive molecules may span across different therapeutic areas, including but not limited to, oncology, neurology, and infectious diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 499995-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,9,9,9 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 499995-79:
(8*4)+(7*9)+(6*9)+(5*9)+(4*9)+(3*5)+(2*7)+(1*9)=268
268 % 10 = 8
So 499995-79-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H19NO5/c1-14(2,3)20-13(19)15-11(8-12(17)18)9-5-4-6-10(16)7-9/h4-7,11,16H,8H2,1-3H3,(H,15,19)(H,17,18)

499995-79-8SDS

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 (3S)-3-(3-hydroxyphenyl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid

1.2 Other means of identification

Product number -
Other names Boc-3-Hydroxy-L-b-phenylalanine

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:499995-79-8 SDS

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