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N-BOC-ISONIPECOTIC ACID is a chemical compound that belongs to the class of organic compounds known as isonicotinic acids. It is specifically classified as a N-acyl-alpha amino acid or derivative. This derivative of isonipecotic acid, an acid naturally occurring in the human body with anticonvulsant and sedative effects, is often utilized as a building block in the synthesis of various organic compounds and pharmaceuticals. Its reactivity and versatile functional groups, along with its unique structure and properties, make N-BOC-ISONIPECOTIC ACID a valuable tool in the design and development of new drugs and materials.

174316-71-3

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174316-71-3 Usage

Uses

Used in Pharmaceutical Industry:
N-BOC-ISONIPECOTIC ACID is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications. Its versatile functional groups allow for the creation of a wide range of molecular structures, enhancing the drug discovery process.
Used in Organic Synthesis:
In the field of organic synthesis, N-BOC-ISONIPECOTIC ACID is used as a building block for the creation of complex organic molecules. Its reactivity and the protection of the amino group by the BOC (tert-butoxycarbonyl) group make it suitable for various synthetic pathways, facilitating the production of desired compounds with specific properties.
Used in Research and Development:
N-BOC-ISONIPECOTIC ACID serves as a valuable research tool in academic and industrial laboratories. It is used in the exploration of new chemical reactions and mechanisms, as well as in the development of innovative materials and drug candidates, thanks to its unique structural features and synthetic utility.
Used in Drug Design:
N-BOC-ISONIPECOTIC ACID is utilized in drug design for its potential to be incorporated into novel molecular entities. Its presence can influence the pharmacokinetic and pharmacodynamic properties of drug candidates, potentially leading to improved efficacy, selectivity, and safety profiles in therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 174316-71-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,3,1 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 174316-71:
(8*1)+(7*7)+(6*4)+(5*3)+(4*1)+(3*6)+(2*7)+(1*1)=133
133 % 10 = 3
So 174316-71-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H19NO4/c1-11(2,3)16-10(15)12-6-4-8(5-7-12)9(13)14/h8H,4-7H2,1-3H3,(H,13,14)/p-1

174316-71-3SDS

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 N-Boc-piperidine-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names N-BOC-ISONIPECOTIC 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:174316-71-3 SDS

174316-71-3Upstream product

174316-71-3Downstream Products

174316-71-3Relevant academic research and scientific papers

Synthesis of (R) and (S) 3-aminoquinuclidine-[3-14C] enantiomers, important components of a variety of 5-HT3 ligands

Parnes,Shelton

, p. 19 - 29 (2007/10/03)

3-Aminoquinuclidine, an important fragment associated with many 5-HT (serotonin) receptor ligands, has been synthesized using a 14C-carbonation based sequence to prepare the starting material, isonicotinic 14C-acid (6). Elaboration of (6) to α-bromoacetyl-[14C] isonipecotic acid (10) via the corresponding diazoketone, followed by intramolecular cyclization, gave the key intermediate 3-quinuclidone-[3-14C] (3). 3-quinuclidone-[3-14C] was converted to a mixture of phenethylamine diastereomers. Carrier free crystallization and hydrogenolysis furnished both (R) and (S) 3-aminoquinuclidine-[3-14C] enantiomers at >99% optical purity.

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