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BOC-(S)-3-AMINO-4-(3-PYRIDYL)-BUTYRIC ACID is a chemical compound characterized by the molecular formula C15H22N2O4. It is a derivative of 3-amino-4-(3-pyridyl)-butyric acid, distinguished by the presence of a BOC protecting group attached to the amino group. BOC-(S)-3-AMINO-4-(3-PYRIDYL)-BUTYRIC ACID plays a significant role in organic synthesis and medicinal chemistry, serving as a key building block for the creation of pharmaceuticals and bioactive molecules. The BOC group's inclusion is strategic, as it manages reactivity and selectivity during chemical reactions, thereby enhancing the compound's utility in crafting complex organic entities. Moreover, the pyridyl group's integration can engender specific interactions in biological contexts, positioning BOC-(S)-3-AMINO-4-(3-PYRIDYL)-BUTYRIC ACID as a promising candidate in drug development and the engineering of biologically active substances.

208404-16-4

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208404-16-4 Usage

Uses

Used in Pharmaceutical Synthesis:
BOC-(S)-3-AMINO-4-(3-PYRIDYL)-BUTYRIC ACID is utilized as a synthetic intermediate for the development of pharmaceuticals, leveraging its structural components to construct a variety of medicinal compounds. The BOC protecting group ensures controlled reactions, facilitating the synthesis of target molecules with precision.
Used in Bioactive Molecule Development:
In the realm of bioactive molecule creation, BOC-(S)-3-AMINO-4-(3-PYRIDYL)-BUTYRIC ACID operates as a fundamental component, contributing to the design of molecules with potential biological activity. The pyridyl group's presence may engender specific binding affinities or reactivities, which are crucial for the molecules' interaction with biological targets.
Used in Organic Synthesis:
BOC-(S)-3-AMINO-4-(3-PYRIDYL)-BUTYRIC ACID is employed as a building block in organic synthesis, where its unique structure allows for the construction of complex organic compounds. BOC-(S)-3-AMINO-4-(3-PYRIDYL)-BUTYRIC ACID's versatility and the strategic use of the BOC protecting group make it an invaluable asset in the synthesis of intricate organic molecules for various applications.
Used in Medicinal Chemistry Research:
BOC-(S)-3-AMINO-4-(3-PYRIDYL)-BUTYRIC ACID is applied as a research tool in medicinal chemistry, where it aids in understanding the structure-activity relationships of potential drug candidates. Its unique structural features, including the BOC protecting group and the pyridyl moiety, make it a valuable probe in exploring novel therapeutic agents and their mechanisms of action.

Check Digit Verification of cas no

The CAS Registry Mumber 208404-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,4,0 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 208404-16:
(8*2)+(7*0)+(6*8)+(5*4)+(4*0)+(3*4)+(2*1)+(1*6)=104
104 % 10 = 4
So 208404-16-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H20N2O4/c1-14(2,3)20-13(19)16-11(8-12(17)18)7-10-5-4-6-15-9-10/h4-6,9,11H,7-8H2,1-3H3,(H,16,19)(H,17,18)/t11-/m0/s1

208404-16-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-(S)-3-amino-4-(3-pyridyl)-butyric acid

1.2 Other means of identification

Product number -
Other names BOC-(S)-3-AMINO-4-(3-PYRIDYL)BUTANOIC 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:208404-16-4 SDS

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