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1-(benzoylamino)cyclopentanecarboxylic acid is a complex organic compound with the molecular formula C13H15NO3. It is a white crystalline solid that is soluble in organic solvents such as ethanol and methanol. 1-(benzoylamino)cyclopentanecarboxylic acid is characterized by a cyclopentane ring, which is fused with a benzene ring through an amide linkage. The carboxylic acid group is attached to the cyclopentane ring, while the benzoyl group is connected to the nitrogen atom of the amide. Due to its unique structure, 1-(benzoylamino)cyclopentanecarboxylic acid has potential applications in the synthesis of pharmaceuticals and other chemical compounds. It is important to note that handling and disposal of this chemical should be done with care, as it may have hazardous properties.

6306-10-1

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6306-10-1 Usage

Structure

Cyclopentanecarboxylic acid derivative with a benzoylamino group attached to the carbon atom

Functional groups

Carboxylic acid group and amine group

Applications

Building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals

Versatility

Can be used as an intermediate in chemical reactions due to the presence of both carboxylic acid and amine groups

Unique structure

Valuable in the creation of complex organic molecules

Potential industries

Wide range of industries, including pharmaceuticals, agrochemicals, and other chemical industries

Check Digit Verification of cas no

The CAS Registry Mumber 6306-10-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6306-10:
(6*6)+(5*3)+(4*0)+(3*6)+(2*1)+(1*0)=71
71 % 10 = 1
So 6306-10-1 is a valid CAS Registry Number.

6306-10-1SDS

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-benzamidocyclopentane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-benzoylamino-cyclopentanecarboxylic 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:6306-10-1 SDS

6306-10-1Relevant academic research and scientific papers

Palladium-Catalyzed Ortho-Alkoxylation of N-Benzoyl α-Amino Acid Derivatives at Room Temperature

Li, Shuangjie,Zhu, Wei,Gao, Feng,Li, Chunpu,Wang, Jiang,Liu, Hong

, p. 126 - 134 (2017/04/26)

An efficient palladium-catalyzed ortho-alkoxylation of N-benzoyl α-amino acid derivatives at room temperature has been explored. This novel transformation, using amino acids as directing groups, Pd(OAc)2 as catalyst, alcohols as the alkoxylation reagents, and PhI(OAc)2 as the oxidant, showed wide generality, good functional tolerance, and high monoselectivity and regioselectivity.

A facile and rapid preparation of hydroxamic acids by hydroxylaminolysis using DBU as base

Beillard, Audrey,Bhurruth-Alcor, Yushma,Bouix-Peter, Claire,Bouquet, Karinne,Chambon, Sandrine,Clary, Laurence,Harris, Craig S.,Millois, Corinne,Mouis, Grégoire,Ouvry, Gilles,Pierre, Romain,Reitz, Arnaud,Tomas, Loic

, p. 2165 - 2170 (2016/05/02)

While there are many protocols for the preparation of hydroxamic acids from their corresponding carboxylic acid or carboxylic ester precursors, most use strong mineral bases that can lead to carboxylic acid impurities that can be difficult to remove using standard chromatographic techniques. This problem is exacerbated when the carbonyl group is hindered. Herein, we communicate a robust hydroxylaminolysis protocol for the preparation of hydroxamic acids in high yield and purity.

A new entry to antihypertensive active pharmaceutical ingredient, Irbesartan and its analogues

Satyanarayana, Bollikonda,Sumalatha, Yasareni,Sridhar, Chaganti,Venkatraman, Sundaram,Reddy, Padi Pratap

, p. 323 - 328 (2007/10/03)

A new synthesis of Irbesartan, an antihypertensive active pharmaceutical ingredient and its analogues is reported.

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