70737-12-1

Basic information

• Product Name: Methyl 2-chloroacetiMidate hydrochloride
• Synonyms: Methyl 2-chloroacetiMidate hydrochloride;Methyl 2-chloroacetiMidate HCl;Methyl 2-chloroethanecarboximidate hydrochloride
• CAS NO: 70737-12-1
• Molecular Formula: C₃H₆ClNO*ClH
• Molecular Weight: 143.99978
• Mol File: 70737-12-1.mol
• Article Data: 10

Chemical Properties

• Melting Point: 77-82°C
• Appearance: /
• Storage Temp.: ?20°C
• CAS DataBase Reference: Methyl 2-chloroacetiMidate hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 2-chloroacetiMidate hydrochloride(70737-12-1)
• EPA Substance Registry System: Methyl 2-chloroacetiMidate hydrochloride(70737-12-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 70737-12-1(Hazardous Substances Data)

Usage

Uses

Reactant for:Modular synthesis of chiral homo- and heterotrisoxazolines as chiral ligands in the asymmetrical Michael addition of indole to benzylidenemalonatePreparation of benzothiazolylthio oxadiazoles

Upstream product

• 107-14-2 chloroacetonitrile 
• 67-56-1 methanol 
• 506-77-4 cyanogen chloride 
• 1634-04-4 tert-butyl methyl ether 

Downstream Products

• 74974-54-2 2-chloro-1,1,1-trimethoxyethane 
• 79-07-2 Chloroacetamide 
• 221196-89-0 (R)-2-(chloromethyl)-4-phenyl-4,5-dihydrooxazole 
• 413597-84-9 (4S)-2-chloromethyl-4-phenyl-2-oxazoline 
• 588701-59-1 (R)-2-(chloromethyl)-4-isopropyl-4,5-dihydrooxazole 
• 252742-72-6 3-(chloromethyl)-1H-1,2,4-triazol-5(4H)-one 
• 221638-74-0 2-(chloromethyl)-6-nitrobenzo[d]oxazole 
• 41014-43-1 2-(chloromethyl)benzoxazole 
• 4760-35-4 2-chloromethyl-1-methyl-1H-benzimidazole 

Relevant articles and documents

Synthetic method of 3-chloromethyl-1,2,4-triazolin-5-one

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

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

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