70737-12-1 Usage
Description
Methyl 2-chloroacetimidate hydrochloride is an organic compound that serves as a valuable reagent in the field of organic synthesis, particularly in the preparation of various heterocyclic compounds and chiral ligands. It is known for its ability to facilitate specific chemical reactions and improve the efficiency of certain synthetic processes.
Uses
Used in Pharmaceutical Industry:
Methyl 2-chloroacetimidate hydrochloride is used as a reactant for the modular synthesis of chiral homoand heterotrisoxazolines. These chiral ligands are essential in the asymmetrical Michael addition of indole to benzylidenemalonate, a crucial reaction in the development of pharmaceutical compounds with improved selectivity and enantiomeric purity.
Used in Chemical Research:
In the field of chemical research, Methyl 2-chloroacetimidate hydrochloride is utilized for the preparation of benzothiazolylthio oxadiazoles, which are important intermediates in the synthesis of various organic compounds and materials. These compounds have potential applications in the development of new drugs, agrochemicals, and other specialty chemicals.
Overall, Methyl 2-chloroacetimidate hydrochloride plays a significant role in the synthesis of complex organic molecules and the development of novel pharmaceutical compounds, making it a valuable asset in both the pharmaceutical industry and chemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 70737-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,3 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70737-12:
(7*7)+(6*0)+(5*7)+(4*3)+(3*7)+(2*1)+(1*2)=121
121 % 10 = 1
So 70737-12-1 is a valid CAS Registry Number.
70737-12-1Relevant articles and documents
Synthetic method of 3-chloromethyl-1,2,4-triazolin-5-one
-
Paragraph 0017; 0018; 0021; 0022, (2019/04/26)
The invention relates to a synthetic method of 3-chloromethyl-1,2,4-triazolin-5-one. The 3-chloromethyl-1,2,4-triazolin-5-one is prepared by mixing chloroacetonitrile, an alcohol and a solvent A. Compared with a conventional process, the synthesis method has the advantages that the raw materials with low price are selected, and production cost is remarkably reduced. For the whole technological process, the synthetic route is shortened, and production efficiency is improved. Production operation and quality control are more convenient while the production process is simplified.
The nitrobenzene structure containing phenylamidines thiazole carboxylic acid amide compound and use thereof
-
Paragraph 0020-0021, (2017/02/24)
The invention relates to the field of medicines related to type II diabetes mellitus and in particular relates to nitrobenzothiazole carboxylic acid amide non-glucoside SGLT (sodium-glucose linked transporter)2/SGLT1 double-target inhibitors containing ph
The structure containing phenylamidines nitrile base benzene thiazole carboxylic acid amides, their preparation and use
-
Paragraph 0018; 0019; 0020; 0021, (2017/04/03)
The invention relates to the field of type 2 diabetes-related medicaments. Specifically, the invention relates to a nitrile benzene thiazolecarboxamide type non-glycoside SGLT2/SGLT1 double-target-point inhibitor containing a phenyl amidine structure, a p