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(2-Chloro-thiazol-5-ylmethyl)-ethyl-amine is a chemical compound characterized by the presence of a thiazole ring with a chlorine atom and an ethyl-amine group. This heterocyclic aromatic ring, coupled with the ethyl-amine functionality, endows the compound with diverse reactivity and potential pharmaceutical applications, making it a valuable building block in the synthesis of various pharmaceuticals and agrochemicals.

120740-07-0

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120740-07-0 Usage

Uses

Used in Pharmaceutical Industry:
(2-Chloro-thiazol-5-ylmethyl)-ethyl-amine is used as a synthetic building block for the development of pharmaceuticals. Its unique structure allows for the creation of amine-based drugs and compounds, which can be utilized in the treatment of various medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, (2-Chloro-thiazol-5-ylmethyl)-ethyl-amine serves as a key component in the synthesis of agrochemicals. Its reactivity and ability to participate in various chemical reactions contribute to the development of effective pesticides and other agricultural products.
Used in Chemical Synthesis:
(2-Chloro-thiazol-5-ylmethyl)-ethyl-amine is employed as a versatile reagent in chemical synthesis. Its diverse reactivity and the presence of the thiazole ring make it suitable for the synthesis of a wide range of molecules, including those with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 120740-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,7,4 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 120740-07:
(8*1)+(7*2)+(6*0)+(5*7)+(4*4)+(3*0)+(2*0)+(1*7)=80
80 % 10 = 0
So 120740-07-0 is a valid CAS Registry Number.

120740-07-0SDS

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 N-[(2-Chloro-1,3-thiazol-5-yl)methyl]ethanamine

1.2 Other means of identification

Product number -
Other names (2-Chloro-thiazol-5-ylmethyl)-ethyl-amine

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:120740-07-0 SDS

120740-07-0Downstream Products

120740-07-0Relevant academic research and scientific papers

Thiazolyl anabasine compound as well as preparation method and application thereof

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Paragraph 0023; 0025; 0027, (2018/09/21)

The invention discloses a thiazolyl anabasine compound as well as a preparation method and application thereof. The structure formula of the thiazolyl anabasine compound is shown as formula I, wherein R1 is hydrogen, methyl or ethyl; R2 is hydrogen, methyl, 2-chlorine-5-thiazole methyl or 6-chlorine-3-picolyl; 2-chlorine-5-chloromethyl thiazole reacts with ethylamine, so as to generate 2-chlorine-5-ethylamine methyl thiazole; and then, 1,1-dichloro nitro ethylene or 1,1,1-trichloronitroethane, 2-chlorine-5-ethylamine methyl thiazole and compound R1NH2R2 react under the existence of alkali, thereby generating the thiazolyl anabasine compound. The thiazolyl anabasine compound disclosed by the invention can be independently prepared into an insecticide and also can be mixed with other pesticides for preparing the insecticide. The thiazolyl anabasine compound disclosed by the invention has the advantages of high insecticidal activity, low toxicity, wide insecticidal spectrum, and the like, and has obvious insecticidal effect for plant hoppers, aphids, and the like.

Substituted benzisothiazole compound and application

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Paragraph 0158; 0160; 0161; 0162, (2018/03/24)

The invention discloses a substituted benzisothiazole compound. R1 is cyan, hydroxyl, C1-C4 alkyl, cyclopropyl, cyanomethyl, methoxyl, ethyoxyl, acetyl, trifluoroacetyl, C1-C4 alkoxycarbonyl and methylsulfonyl or ethylsulfonyl, R2 is independently selected from hydrogen, halogen, cyan, methyl, methoxyl, trifluoromethyl and trifluoromethoxyl or difluoromethoxyl, n is 1, 2, 3 or 4, m is 1 or 2, and J is replaced thiazole, isothiazole or pyridine. The compound has excellent activity and good plant tolerance and environmental safety under low concentration and can inhibit or destroy various pathogenic fungi and bacteria generated by plants or soil and kill various insect pests and mites, and sterilization and insecticidal spectrums of the compound are widened. According to the preparation method, used raw materials are economical and easy to get, and the preparation method is high in yield and low in synthesis process cost and has good sterilization activity and pest and mite killing activity.

Thiazole Methylamino Pyridine Compounds and Preparation Method Therefor

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Paragraph 0060-0061, (2015/02/25)

Disclosed are thiazole methylamino pyridine compounds represented by the general formula (I) having fungicidal, insecticidal/acaricidal, and herbicidal activity, the preparation method thereof, the fungicidal, insecticidal/acaricidal, and herbicidal compositions containing the compounds of the present invention, and the use and the method for controlling fungi, insects/acari and weeds of the compounds of the present invention.

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