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2-PIPERIDINOBENZAMIDE, with the molecular formula C12H16N2O, is a benzamide derivative featuring a piperidine substituent. This chemical compound is characterized by a six-membered heterocyclic ring containing five carbon atoms and one nitrogen atom, which is integral to its structure. It is widely recognized as a fundamental building block in the realms of organic synthesis and medicinal chemistry, attributed to its unique structural and property attributes.

3430-40-8

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3430-40-8 Usage

Uses

Used in Pharmaceutical Industry:
2-PIPERIDINOBENZAMIDE is utilized as a key component in the development of pharmaceutical drugs due to its distinctive structural features. Its incorporation in drug design facilitates the creation of novel therapeutic agents, potentially enhancing the efficacy and selectivity of medications.
Used in Organic Synthesis:
In the field of organic synthesis, 2-PIPERIDINOBENZAMIDE serves as a valuable intermediate. Its presence in the synthesis process allows for the construction of complex organic molecules, contributing to the advancement of chemical research and the development of new compounds with diverse applications.
Used in Agrochemicals:
2-PIPERIDINOBENZAMIDE is also employed as a starting material in the synthesis of agrochemicals. Its role in this industry is pivotal for the creation of new pesticides, herbicides, and other agricultural chemicals, thereby supporting agricultural productivity and crop protection.

Check Digit Verification of cas no

The CAS Registry Mumber 3430-40-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,3 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3430-40:
(6*3)+(5*4)+(4*3)+(3*0)+(2*4)+(1*0)=58
58 % 10 = 8
So 3430-40-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2O/c13-12(15)10-6-2-3-7-11(10)14-8-4-1-5-9-14/h2-3,6-7H,1,4-5,8-9H2,(H2,13,15)

3430-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-piperidin-1-ylbenzamide

1.2 Other means of identification

Product number -
Other names 2-piperidinobenzamide

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:3430-40-8 SDS

3430-40-8Downstream Products

3430-40-8Relevant academic research and scientific papers

Efficient construction of C=N double bonds via acceptorless dehydrogenative coupling

Sun, Xiang,Hu, Yu,Nie, Shao-Zhen,Yan, Yun-Yun,Zhang, Xue-Jing,Yan, Ming

, p. 2179 - 2184 (2013/10/01)

The efficient construction of C=N double bonds has been achieved by the Ir-catalyzed intramolecular acceptorless dehydrogenative cross-coupling of tertiary amines and amides. An iridium/2-hydroxypyridine complex was identified as the highly efficient catalyst. A number of quinazolinone derivatives was prepared in excellent yields. An iridium-mediated C-H activation mechanism is proposed. This finding provides an unprecedented strategy for the direct imidation of sp3 C-H bonds.

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