Welcome to LookChem.com Sign In|Join Free

CAS

  • or
1-Benzenoyl-piperidine-2-carboxylic acid, also known as BP-Carboxylic Acid, is a versatile chemical compound belonging to the class of carboxylic acids. It is a derivative of piperidine, a heterocyclic organic compound, featuring a benzoyl group. BP-Carboxylic Acid has been studied for its potential pharmacological properties, such as enzyme inhibition and its role as a building block for the synthesis of other compounds. Additionally, it has been investigated for its potential use in the development of pharmaceuticals and as a ligand in metal coordination chemistry.

78348-46-6

Post Buying Request

78348-46-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

78348-46-6 Usage

Uses

Used in Pharmaceutical Development:
1-Benzenoyl-piperidine-2-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable building block for the development of new drugs with potential therapeutic applications.
Used in Enzyme Inhibition:
BP-Carboxylic Acid is used as an enzyme inhibitor, leveraging its ability to bind and modulate the activity of specific enzymes. This property can be harnessed to develop drugs targeting enzyme-related diseases and conditions.
Used in Metal Coordination Chemistry:
1-Benzenoyl-piperidine-2-carboxylic acid is used as a ligand in metal coordination chemistry, enabling the formation of stable complexes with various metal ions. This application can lead to the development of new materials with unique properties and potential uses in different industries.
Used in Chemical Research:
BP-Carboxylic Acid serves as a valuable compound in chemical research, providing insights into the structure, properties, and potential applications of carboxylic acid derivatives and heterocyclic compounds. Its study contributes to the advancement of knowledge in the fields of organic and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 78348-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,3,4 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78348-46:
(7*7)+(6*8)+(5*3)+(4*4)+(3*8)+(2*4)+(1*6)=166
166 % 10 = 6
So 78348-46-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO3/c15-12(10-6-2-1-3-7-10)14-9-5-4-8-11(14)13(16)17/h1-3,6-7,11H,4-5,8-9H2,(H,16,17)

78348-46-6SDS

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 1-benzoylpiperidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names DL-N-benzoylpipecolinic 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:78348-46-6 SDS

78348-46-6Relevant articles and documents

Beauveria bassiana ATCC 7159 contains an L-specific α-amino acid benzamidase

Holland, Herbert L.,Andreana, Peter R.,Salehzadeh-Asl, Reza,Van Vliet, Aaron,Ihasz, Nancy J.,Brown, Frances M.

, p. 667 - 672 (2007/10/03)

Biotransformation of a series of racemic N-benzoyl α-amino acids by the fungus Beauveria bassiana ATCC 7159 results in isolation of the corresponding D-amino acid benzamides in high enantiomeric purity and yield.

Photochemical reaction between tertiary allylic amines and chromium carbene complexes: Synthesis of lactams via a zwitterion aza cope rearrangement

Deur, Christopher J.,Miller, Michael W.,Hegedus, Louis S.

, p. 2871 - 2876 (2007/10/03)

Photolysis of chromium carbene complexes in the presence of tertiary allylic amines resulted in a zwitterionic aza Cope rearrangement to produce unsaturated lactams in fair yield.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 78348-46-6