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
• Article Data: 5

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

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

Downstream Products

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

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.

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.