94052-40-1

Basic information

• Product Name: methyl cyclohexanecarboximidate hydrochloride
• Synonyms: methyl cyclohexanecarboximidate hydrochloride
• CAS NO: 94052-40-1
• Molecular Weight: 177.674
• Mol File: 94052-40-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: methyl cyclohexanecarboximidate hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: methyl cyclohexanecarboximidate hydrochloride(94052-40-1)
• EPA Substance Registry System: methyl cyclohexanecarboximidate hydrochloride(94052-40-1)

Safety Data

• Hazardous Substances Data: 94052-40-1(Hazardous Substances Data)

Upstream product

• 1855-63-6 cyclohex-1-enecarbonitrile 
• 67-56-1 methanol 
• 766-05-2 cyclohexane carbonitrile 
• 32379-37-6 1-Acetoxy-cyclohexylcyanid 

Downstream Products

• 51354-80-4 cyclohexanorthocarboxylic acid trimethyl ester 
• 4630-82-4 methyl cyclohexylcarboxylate 
• 1122-56-1 cyclohexylcarboxamide 
• 66823-00-5 2-cyclohexyl-2-methoxy-[1,3]dioxolane 
• 91959-21-6 4-(5-cyclohexyl-[1,3,4]oxadiazol-2-yl)-pyridine 
• 99355-54-1 methyl N-(1-methoxy-2-phenylethyl)cyclohexanecarboximidate 
• 2498-48-8 cyclohexanecarboximidamide hydrochloride 
• 155884-31-4 4-carbomethoxy-2-cyclohexyl-2-oxazoline 
• 26059-80-3 2-cyclohexylquinazolin-4(3Η)-one 
• 284486-58-4 2-cyclohexyl-4-chloroquinazoline 
• 155884-27-8 methyl 2-cyclohexyloxazole-4-carboxylate 
• 99355-62-1 Cyclohexanecarboxylic acid (1-methoxy-2,2-dimethyl-propyl)-amide 
• 99355-55-2 N-(-1-methoxy-2-phenylethyl)cyclohexanecarboxamide 
• 24722-30-3 cyclohexanecarboximidamide 

Relevant articles and documents

One-pot synthesis of 2,5-disubstituted pyrimidines from nitriles

A practical, one-step process for the synthesis of 2,5-disubstituted pyrimidines is presented. The protocol proved to be general for the synthesis of a variety of pyrimidine-containing compounds bearing an assortment of functional groups.

A facile and versatile route to 2-substituted-4(3H)-quinazolinones and quinazolines

A range of 2-aryl and 2-alkyl quinazolinones have been prepared in moderate to good yields from the reaction of anthranilic acid and the appropriately substituted imidate in a facile, mild, onepot procedure. Subsequent reaction with phosphorus oxychloride afforded the corresponding 4-chloro-2-substituted quinazolines, which are useful synthetic intermediates, in good to high yields. Product isolation was facilitated by the development of work up procedures for both reactions that did not include purification by column chromatography.

Heterocyclic amplifiers of phleomycin. IV. Pyrimidinylpurines, phenylpyrimidines and related systems with basic side chains

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