17091-40-6

Basic information

• Product Name: 2-isobutylaminoethanol
• Synonyms: 2-isobutylaminoethanol;2-(isobutylamino)ethanol(SALTDATA: HCl)
• CAS NO: 17091-40-6
• Molecular Formula: C₆H₁₅NO
• Molecular Weight: 117.1894
• EINECS: 241-159-8
• Mol File: 17091-40-6.mol

Chemical Properties

• Melting Point: 28.94°C (estimate)
• Boiling Point: 219.03°C (rough estimate)
• Flash Point: 72.1°C
• Appearance: /
• Density: 0.8818
• Vapor Pressure: 0.0852mmHg at 25°C
• Refractive Index: 1.4402
• CAS DataBase Reference: 2-isobutylaminoethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-isobutylaminoethanol(17091-40-6)
• EPA Substance Registry System: 2-isobutylaminoethanol(17091-40-6)

Safety Data

• Hazardous Substances Data: 17091-40-6(Hazardous Substances Data)

Usage

Hazard

A poison.

InChI:InChI=1/C6H15NO/c1-6(2)5-7-3-4-8/h6-8H,3-5H2,1-2H3

Upstream product

• 75-21-8 oxirane 
• 78-81-9 isobutylamine 
• 27035-32-1 2-isopropyltetrahydro-1,3-oxazole 
• 78-77-3 Isobutyl bromide 
• 141-43-5 ethanolamine 
• 78-84-2 isobutyraldehyde 
• 141-46-8 Glycolaldehyde 
• 80066-51-9 N-isobutyl-2,2-pentamethylene-1,3-oxazolidine 
• 95759-31-2 2-(N-isopropylidene)aminoethanol 

Downstream Products

• 19170-50-4 4-methylamino-benzoic acid-(2-isobutylamino-ethyl ester) 
• 92727-03-2 4-ethoxy-benzoic acid-(2-isobutylamino-ethyl ester); hydrochloride 
• 19170-51-5 4-ethylamino-benzoic acid-(2-isobutylamino-ethyl ester) 
• 63957-01-7 fluorene-9-carboxylic acid-(2-isobutylamino-ethyl ester); hydrochloride 
• 4535-66-4 2-(diisobutylamino)ethanol 

Relevant articles and documents

Daisy chain assembly formed from a cucurbit[6]uril derivative

The building block synthesis of a derivative of CB[6] that bears a reactive propargyloxy group and its functionalization by click chemistry to yield 1 which contains a covalently attached isobutylammonium group is presented. Compound 1 undergoes self-assembly to yield a cyclic [c2] daisy chain assembly (12) in water. The behavior of 12 in response to various stimuli (e.g., guests and CB[n] receptors) is described.

A practical synthesis of N-alkyl- and N,N′-dialkyl-polyamines This work is dedicated to the memory of our dear colleague and friend Mr. Charles Edward Price

A variety of polyamines have been synthesized from their corresponding amino alcohols through a 3-step process. The synthesis predicates that the most likely impurities are of higher molecular weight and that distillation is effective at producing highly pure materials. This sequence is scalable, requires no protecting groups or chromatography, and provides the requisite polyamines in moderate to good yields.

PHOSPHONOOXY QUINAZOLINE DERIVATIVES AND THEIR PHARMACEUTICAL USE

Quinazoline derivatives of formula (I) wherein A is 5-membered heteroaryl containing a nitrogen atom and one or two further nitrogen atoms; compositions containing them, processes for their preparation and their use in therapy.

OXAZOLIDINES. 1. BASIC CATALYTIC DISPROPORTIONATION OF CYCLOHEXANOSPIRO-2-OXAZOLIDINES: SYNTHESIS OF N-SUBSTITUTED 4,5,6,7-TETRAHYDROINDOLES

It has been shown that the basic catalytic disproportionation of cyclohexanospiro-2-oxazolidines in the presence of potasium hydroxide or sodium methylate leads to N-substituted 4,5,6,7-tetrahydroindoles with a yield of up to 73percent.The influence of the character of substituents at the nitrogen atom of oxazolidine on the course of the reaction has been established.