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3-N-BOC-AMINO-4-IODO-6-PHENYLPYRIDINE is a pyridine-based chemical compound featuring a substituted pyridine ring with a BOC-protected amino group at the 3-position, an iodine atom at the 4-position, and a phenyl group at the 6-position. The BOC (tert-butyloxycarbonyl) group serves as a protecting agent for the amine group, making 3-N-BOC-AMINO-4-IODO-6-PHENYLPYRIDINE a versatile building block in organic synthesis for the development of pharmaceuticals, agrochemicals, and materials. Its unique structure and functional groups also suggest potential applications in medicinal chemistry and drug discovery.

941271-13-2

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941271-13-2 Usage

Uses

Used in Pharmaceutical Synthesis:
3-N-BOC-AMINO-4-IODO-6-PHENYLPYRIDINE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex molecular structures. The BOC-protected amino group allows for selective reactions to occur at other sites on the molecule, facilitating the creation of diverse drug candidates.
Used in Agrochemical Development:
In the agrochemical industry, 3-N-BOC-AMINO-4-IODO-6-PHENYLPYRIDINE is utilized as a building block for the development of new pesticides and herbicides. Its structural features can be tailored to target specific pests or weeds, potentially leading to more effective and environmentally friendly products.
Used in Medicinal Chemistry Research:
3-N-BOC-AMINO-4-IODO-6-PHENYLPYRIDINE serves as a valuable compound in medicinal chemistry research, where it can be used to explore the structure-activity relationships of potential drug molecules. Its unique substitution pattern may offer insights into the design of novel therapeutic agents.
Used in Drug Discovery:
3-N-BOC-AMINO-4-IODO-6-PHENYLPYRIDINE is employed in drug discovery processes to identify new lead compounds with potential therapeutic effects. The iodine and phenyl groups, in particular, may impart specific biological activities that can be optimized through further chemical modifications.
Used in Material Science:
3-N-BOC-AMINO-4-IODO-6-PHENYLPYRIDINE can also be used in material science for the development of new materials with unique properties. Its ability to form complexes or participate in polymerization reactions could lead to advances in areas such as sensors, catalysts, or advanced materials with tailored properties.

Check Digit Verification of cas no

The CAS Registry Mumber 941271-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,1,2,7 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 941271-13:
(8*9)+(7*4)+(6*1)+(5*2)+(4*7)+(3*1)+(2*1)+(1*3)=152
152 % 10 = 2
So 941271-13-2 is a valid CAS Registry Number.

941271-13-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(4-iodo-6-phenylpyridin-3-yl)carbamate

1.2 Other means of identification

Product number -
Other names 3-N-Boc-Amino-4-iodo-6-phenylpyridine

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:941271-13-2 SDS

941271-13-2Downstream Products

941271-13-2Relevant academic research and scientific papers

1,1,1-TRIFLUORO-4-PHENYL-4-METHYL-2-(1H-PYRROLO

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Page/Page column 171-172, (2010/02/11)

Compounds of Formula (IA), IB), IC), and (ID) wherein R1, R2, R3, R4, R5, and R6 are as respectively defined herein for Formula (IA), (IB), (IC), and (ID), or a tautomer, prodrug, solvate, or salt thereof; pharmaceutical compositions containing such compounds, and methods of modulating the glucocorticoid receptor function and methods of treating disease-states or conditions mediated by the glucocorticoid receptor function or characterized by inflammatory, allergic, or proliferative processes in a patient using these compounds.

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