120740-06-9 Usage
Uses
Used in Medicinal Chemistry:
(2-Chloro-thiazol-5-ylMethyl)-Methyl-aMine is used as a building block for the synthesis of biologically active molecules due to its unique structural features, including the chloro-thiazole and methyl groups. Its presence in medicinal chemistry allows for the development of new drugs with potential therapeutic applications.
Used in Pharmaceutical Research:
In pharmaceutical research, (2-Chloro-thiazol-5-ylMethyl)-Methyl-aMine is utilized for its ability to participate in various biological processes within living organisms. The amine group in (2-Chloro-thiazol-5-ylMethyl)-Methyl-aMine enables it to form important chemical reactions, making it a valuable component in the discovery and development of novel pharmaceutical agents.
Used in Drug Synthesis:
(2-Chloro-thiazol-5-ylMethyl)-Methyl-aMine is used as a key intermediate in the synthesis of various drugs. Its unique chemical properties allow it to be incorporated into the molecular structures of potential therapeutic agents, contributing to their biological activity and efficacy.
Used in Chemical Reactions:
(2-Chloro-thiazol-5-ylMethyl)-Methyl-aMine is also used in various chemical reactions due to the reactivity of its amine group. The ability of the amine group to form bonds and participate in reactions makes (2-Chloro-thiazol-5-ylMethyl)-Methyl-aMine a versatile component in organic synthesis and other chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 120740-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,7,4 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 120740-06:
(8*1)+(7*2)+(6*0)+(5*7)+(4*4)+(3*0)+(2*0)+(1*6)=79
79 % 10 = 9
So 120740-06-9 is a valid CAS Registry Number.
120740-06-9Relevant academic research and scientific papers
Substituted benzisothiazole compound and application
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Paragraph 0148; 0150; 0153; 0154, (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.
Butenone compounds, their preparation and their use as pesticides
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, (2008/06/13)
A butenone compound having the general formula I: STR1 wherein R1 represents a pyridyl or thiazolyl group bearing one or more substituents independantly selected from halogen atoms, alkyl, alkoxy, alkylthio, haloalkyl, cyano, alkoxycarbonyl, alkylamino and dialkylamino; R2 represents a hydrogen atom, an alkyl group or an alkylcarbonyl group; R3 represents an alkyl group; R4 represents a haloalkyl group; X represents a sulphur atom or a group of formula N--R5, wherein R5 represents a hydrogen atom, an alkyl group or an alkylcarbonyl group; and n is 0 or 1, methods for their preparation and their use in combating pests.
