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14753-26-5

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14753-26-5 Usage

General Description

3-Chloropropylamine is an alkyl amine compound with the chemical formula C3H8ClN. It is a colorless to pale yellow liquid with a strong, ammonia-like odor. This chemical is commonly used as an intermediate in the production of pharmaceuticals, agricultural chemicals, and other organic compounds. It is also utilized in the preparation of catalysts and as a reagent in chemical synthesis. 3-Chloropropylamine is flammable and can form explosive mixtures with air, so it should be handled with caution and stored in a cool, well-ventilated area. Additionally, it is toxic if inhaled, swallowed, or absorbed through the skin, and can cause irritation to the respiratory system, skin, and eyes. Therefore, proper safety measures should be taken when working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 14753-26-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,5 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14753-26:
(7*1)+(6*4)+(5*7)+(4*5)+(3*3)+(2*2)+(1*6)=105
105 % 10 = 5
So 14753-26-5 is a valid CAS Registry Number.

14753-26-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloropropan-1-amine

1.2 Other means of identification

Product number -
Other names 3-chloro-1-aminopropane

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:14753-26-5 SDS

14753-26-5Relevant articles and documents

A Facile Strategy for the Construction of Cyclic Peptoids under Microwave Irradiation through a Simple Substitution Reaction

Kaniraj, Prathap Jeya,Maayan

, p. 2110 - 2113 (2015)

We describe a fast and efficient side chain-to-tail cyclization of N-substituted glycine oligomers, peptoids, on a solid support and under microwave irradiation. We demonstrate that cyclic peptoids varied in their ring size and side chains can be synthesized by a bond formation between a chloropropyl group placed anywhere along the sequence and the secondary amine at the N-terminus. This SN2 reaction leads to the formation of a new C-N bond using only one reagent (a base). (Chemical Equation Presented).

Facile method for the synthesis of triazole- and tetrazole-containing peptoids on a solid support

Lee, Yen Jea,Kang, Dahyun,Seo, Jiwon

, p. 3311 - 3316 (2018)

The late-stage functionalization of a biomimetic foldamer such as a peptoid is a useful tool to achieve structural diversity. Herein, a facile method for the synthesis of triazole- or tetrazole-containing peptoids using post-synthetic modifications has been reported. On a resin-bound peptoid with a chloroalkyl side chain(s), substitution with nucleophiles (azide or cyanide) and the subsequent [3 + 2]-cycloaddition reaction were optimized. Peptoids with azide, triazole, and tetrazole functional groups could be readily synthesized and could potentially be utilized further for orthogonal bioconjugation or metal recognition.

Copper (II) complexes with tetradentate N4 and N2S2 ligands: effect of ligands on redox behavior and EPR parameters. Superoxide dismutase-like activity

Chautemps, Pierre,Gellon, Gisele,Morin, Benedicte,Pierre, Jean-Louis,Provent, Christophe,et al.

, p. 434 - 443 (2007/10/02)

Nine copper (II) complexes with tetradentate N4 and N2S2 (open chain or macrocyclic) ligands were prepared and studied in solution.For comparison, one N2O2 and one N3S ligand were included.EPR studies evidenced the stereochemistry around the copper (II) ion (square planar or tetrahedrally distorted).The redox or reduction potentials were obtained from electrochemical studies.UV-visible spectra gave additional information on the stereochemistry of the complexes and the deprotonation of amide ligands.The effect of ligands on redox behavior and stereochemistry is dicussed.Superoxide dismutase (SOD) activities were evidenced for the 11 complexes by spin-trapping method and by NBT assay.Unfortunately, the SOD activities do not survive bovine serum albumin in solution. - Keywords: Cu (II) complexes; EPR spectroscopy; electrochemistry; UV-visible spectroscopy; superoxide dismutase activity.

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