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4-[(2-Chloroethyl)ethylamino]-benzaldehyde is an organic compound characterized by a benzene ring with a formyl group and an aminoethyl group. It features a chlorine atom attached to one of the carbon atoms in the aminoethyl group, contributing to its unique chemical properties. Known by its chemical formula C10H12ClNO, 4-[(2-Chloroethyl)ethylamino]-benzaldehyde serves as a versatile intermediate in the synthesis of pharmaceuticals and other organic compounds, as well as a reagent in chemical reactions for the formation of amine and aldehyde derivatives.

2643-07-4

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2643-07-4 Usage

Uses

Used in Pharmaceutical Industry:
4-[(2-Chloroethyl)ethylamino]-benzaldehyde is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic chemistry, 4-[(2-Chloroethyl)ethylamino]-benzaldehyde is utilized as a reagent for the formation of amine and aldehyde derivatives, which are essential building blocks in the creation of complex organic molecules.
Used in Chemical Research:
4-[(2-Chloroethyl)ethylamino]-benzaldehyde is employed in chemical research to explore its reactivity and potential applications in the synthesis of novel compounds, contributing to the advancement of chemical knowledge and innovation.

Check Digit Verification of cas no

The CAS Registry Mumber 2643-07-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,4 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2643-07:
(6*2)+(5*6)+(4*4)+(3*3)+(2*0)+(1*7)=74
74 % 10 = 4
So 2643-07-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H14ClNO/c1-2-13(8-7-12)11-5-3-10(9-14)4-6-11/h3-6,9H,2,7-8H2,1H3

2643-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-chloroethyl(ethyl)amino]benzaldehyde

1.2 Other means of identification

Product number -
Other names -

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:2643-07-4 SDS

2643-07-4Relevant academic research and scientific papers

A series of water-soluble photosensitizers based on 3-cinnamoylcoumarin for: In vitro antimicrobial photodynamic inactivation

Sun, Zhiyuan,Zhou, Shaona,Qiu, Haixia,Gu, Ying,Zhao, Yuxia

, p. 17073 - 17078 (2018/05/29)

A series of novel water-soluble photosensitizers (PSs; M1-M5) based on 3-cinnamoylcoumarin derivatives, incorporating carboxylic acid salt (M1, M2), pyridine salt (M3, M4) and quaternary ammonium salt (M5) groups, were designed and synthesized. Their phot

Water-soluble cationic benzylidene cyclopentanone photosensitizer and preparation method and application of photosensitizer in photodynamic sterilization

-

Paragraph 0121; 0122; 0123, (2017/07/26)

The invention discloses a water-soluble cationic benzylidene cyclopentanone photosensitizer and a synthetic method and application of the photosensitizer in photodynamic sterilization. The photosensitizer has a simple molecular structure, has a determined

Cationic benzylidene cyclopentanone photosensitizers for selective photodynamic inactivation of bacteria over mammalian cells

Fang, Yanyan,Liu, Tianlong,Zou, Qianli,Zhao, Yuxia,Wu, Feipeng

, p. 56067 - 56074 (2015/07/15)

To inactivate both standard strains as well as antibiotic-resistant strains of bacteria with minimum damage to host cells, three new pyridyl cationic-modified benzylidene cyclopentanone photosensitizers (PSs), P1 (with one cationic group), P2 (with two ca

Near-infrared solid-state emitters based on isophorone: Synthesis, crystal structure and spectroscopic properties

Massin, Julien,Dayoub, Wissam,Mulatier, Jean-Christophe,Aronica, Christophe,Bretonniere, Yann,Andraud, Chantal

experimental part, p. 862 - 873 (2012/02/14)

A series of near-infrared solid-state emitters based on the dicyanoisophorone electron acceptor group was synthesized. The solid-state spectroscopic properties were studied by UV-visible absorption spectroscopy and fluorescence spectroscopy and analyzed i

Prodrugs for selective drug delivery

-

, (2008/06/13)

A broad class of pharmaceutical agents which react directly with electron carriers or with reactive species produced by electron transport to release a pharmacologically active molecule to effect a therapeutic functional change in the organism by a receptor or nonrecepter mediated action.

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