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2-Piperidinecarboxylic acid, 1-acetyl-, (R)(9CI), also known as (R)-1-acetylpiperidine-2-carboxylic acid, is a chiral chemical compound with the molecular formula C8H13NO3. It is a derivative of piperidine and serves as an intermediate in the synthesis of various pharmaceuticals and organic compounds. 2-Piperidinecarboxylic acid, 1-acetyl-, (R)(9CI) is of interest in the pharmaceutical and chemical industries due to its versatile properties and its role as a building block in organic chemistry synthesis.

178963-27-4

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178963-27-4 Usage

Uses

Used in Pharmaceutical Industry:
2-Piperidinecarboxylic acid, 1-acetyl-, (R)(9CI) is used as an intermediate in the synthesis of drug molecules for various therapeutic applications. Its unique chiral properties allow for the development of enantiomer-specific medications, which can have different biological activities and reduce potential side effects.
Used in Organic Chemistry Synthesis:
In the field of organic chemistry, 2-Piperidinecarboxylic acid, 1-acetyl-, (R)(9CI) is utilized as a building block for the creation of complex organic compounds. Its versatile structure makes it a valuable component in the synthesis of a wide range of molecules, including those with potential applications in materials science, agrochemicals, and other specialty chemical markets.

Check Digit Verification of cas no

The CAS Registry Mumber 178963-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,9,6 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 178963-27:
(8*1)+(7*7)+(6*8)+(5*9)+(4*6)+(3*3)+(2*2)+(1*7)=194
194 % 10 = 4
So 178963-27-4 is a valid CAS Registry Number.

178963-27-4SDS

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 2-Piperidinecarboxylic acid, 1-acetyl-, (R)- (9CI)

1.2 Other means of identification

Product number -
Other names (R)-1-Acetyl-2-piperidinecarboxylic 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:178963-27-4 SDS

178963-27-4Downstream Products

178963-27-4Relevant academic research and scientific papers

β-Lactamase inhibition profile of new amidine-substituted diazabicyclooctanes

Iqbal, Zafar,Zhai, Lijuan,Gao, Yuanyu,Tang, Dong,Ma, Xueqin,Ji, Jinbo,Sun, Jian,Ji, Jingwen,Liu, Yuanbai,Jiang, Rui,Mu, Yangxiu,He, Lili,Yang, Haikang,Yang, Zhixiang

supporting information, p. 711 - 718 (2021/04/09)

The diazabicyclooctane (DBO) scaffold is the backbone of non-β-lactam-based second generation β-lactamase inhibitors. As part of our efforts, we have synthesized a series of DBO derivatives A1–23 containing amidine substituents at the C2 position of the bicyclic ring. These compounds, alone and in combination with meropenem, were tested against ten bacterial strains for their antibacterial activity in vitro. All compounds did not show antibacterial activity when tested alone (MIC >64 mg/L), however, they exhibited a moderate inhibition activity in the presence of meropenem by lowering its MIC values. The compound A12 proved most potent among the other counterparts against all bacterial species with MIC from a MIC value of 0.125 mg/L.

CYCLIC AMINE DERIVATIVE AND MEDICAL USE THEREOF

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Paragraph 0398-0403, (2020/12/25)

A cyclic amine derivative represented by general Formula (I): wherein R1 represents an alkyl group having 1 to 3 carbon atoms; A represents a group represented by general Formula (II-1), (II-2), or (II-3): R2 represents a hydrogen at

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