3719-52-6

Basic information

• Product Name: (1-nitrocyclohexyl)methanol
• Synonyms: (1-nitrocyclohexyl)methanol
• CAS NO: 3719-52-6
• Molecular Weight: 159.185
• Mol File: 3719-52-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (1-nitrocyclohexyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1-nitrocyclohexyl)methanol(3719-52-6)
• EPA Substance Registry System: (1-nitrocyclohexyl)methanol(3719-52-6)

Safety Data

• Hazardous Substances Data: 3719-52-6(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 1122-60-7 1-nitrocyclohexane 
• 71481-64-6 formaldehyde(methanol 44%, water 10%) 
• 29788-20-3 1-bromo-1-nitrocyclohexane 

Downstream Products

• 81467-34-7 3-oxa-1-azaspiro[4.5]decan-2-one 
• 90204-86-7 N-(1-hydroxymethyl-cyclohexyl)-formamide 
• 53104-35-1 N-(1-(hydroxymethyl)cyclohexyl)acetamide 
• 100400-91-7 1-acetoxymethyl-1-acetylamino-cyclohexane 
• 101725-44-4 N₁,N₂-bis(1-(hydroxymethyl)cyclohexyl)oxalamide 
• 102449-45-6 1-benzoylamino-1-benzoyloxymethyl-cyclohexane 
• 4368-61-0 1-(dimethylamino)-1-cyclohexanecarbinol 
• 1258978-47-0 2-((1-nitrocyclohexyl)methylamino)-2-(hydroxymethyl)propane-1,3-diol 
• 1198151-43-7 3-(vinyloxy)-N-(1-nitrocyclohexylmethyl)propan-1-amine 
• 1198151-42-6 2-(vinyloxy)-N-(1-nitrocyclohexylmethyl)ethanamine 
• 1121-50-2 1-(chloromethylene)cyclohexane 
• 98432-02-1 1-nitro-cyclohexanecarboxylic acid 
• 4313-56-8 (1-aminocyclohexyl)methanol 
• 105-60-2 caprolactam 

Relevant articles and documents

Preparation of indium nitronates and their Henry reactions

Indium nitronates were readily prepared from commercially available nitroalkanes by transmetallation of the corresponding lithium nitronates with indium salts. The Henry reaction of this indium organometallics with aldehydes afforded β-nitroalkanols in moderate to high yields. The use of chiral sugar aldehydes furnished the corresponding carbohydrate-derived β-nitroalkanols with excellent stereoselectivity.

PROCESS FOR MAKING TERTIARY AMINOALCOHOL COMPOUNDS

Provided is a process for making a tertiary aminoalcohol compound. The process comprises using an excess amount of a carbonyl compound in a condensation step between the carbonyl compound and a nitroalkane, and conducting a hydrogenation/alkylation step to produce the tertiary aminoalcohol. The process uses fewer steps than conventional processes.

AMINOALCOHOL AND BIOCIDE COMPOSITIONS FOR AQUEOUS BASED SYSTEMS

Biocidal compositions and their use in aqueous media, such as metalworking fluids, the compositions comprising a biocidal agent; and a non-biocidal primary amino alcohol compound of the formula (I): wherein R1, R2, R3, R4, and R5 are as defined herein.