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125483-56-9

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125483-56-9 Usage

General Description

Cyclobutanecarboxylic acid, 1-amino-, phenylmethyl ester (9CI) is a chemical compound with the molecular formula C12H15NO2. It is an ester derivative of cyclobutanecarboxylic acid containing an amino group and a phenylmethyl group. Cyclobutanecarboxylic acid, 1-amino-, phenylmethyl ester (9CI) has potential applications in the field of organic chemistry, as well as in the pharmaceutical and biotechnology industries. Further research and studies are necessary to understand the specific properties and potential uses of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 125483-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,4,8 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 125483-56:
(8*1)+(7*2)+(6*5)+(5*4)+(4*8)+(3*3)+(2*5)+(1*6)=129
129 % 10 = 9
So 125483-56-9 is a valid CAS Registry Number.

125483-56-9SDS

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 benzyl 1-aminocyclobutane-1-carboxylate

1.2 Other means of identification

Product number -
Other names Cyclobutanecarboxylic acid,1-amino-,phenylmethyl ester

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:125483-56-9 SDS

125483-56-9Relevant articles and documents

Binaphthyl-anchored antibacterial tripeptide derivatives with hydrophobic C-terminal amino acid variations

Bremner, John B.,Keller, Paul A.,Pyne, Stephen G.,Robertson, Mark J.,Sakthivel,Somphol, Kittiya,Baylis, Dean,Coates, Jonathan A.,Deadman, John,Jeevarajah, Dharshini,Rhodes, David I.

, p. 1265 - 1270 (2012/09/25)

The facile synthesis of seven new dicationic tripeptide benzyl ester derivatives, with hydrophobic group variations in the C-terminal amino acid component, is described. Moderate to good activity was seen against Gram-positive bacteria in vitro. One cyclohexylsubstituted compound 2c was tested more widely and showed good potency (MIC values ranging from 2-4 μg/mL) against antibiotic-resistant strains of Staphylococcus aureus and Enterococci (VRE, VSE), and against Staphylococcus epidermidis.

1-CARBAMOYLCYCLOALKYLCARBOXYLIC ACID COMPOUNDS, PROCESSES FRO MAKING AND USES THEREOF

-

Page/Page column 19, (2008/06/13)

The invention relates to the field of pharmaceutics and more specifically to novel cycloalkylamidoacid compositions useful in the preparation of cycloalkyaminoacids and oxazolidinediones, and processes for making cycloamidoacids. Formula (1)

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