164226-14-6

Basic information

• Product Name: 4-isopropyl-N-tert-butoxycarbonylaniline
• Synonyms: 4-isopropyl-N-tert-butoxycarbonylaniline
• CAS NO: 164226-14-6
• Molecular Weight: 235.326
• Mol File: 164226-14-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 4-isopropyl-N-tert-butoxycarbonylaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-isopropyl-N-tert-butoxycarbonylaniline(164226-14-6)
• EPA Substance Registry System: 4-isopropyl-N-tert-butoxycarbonylaniline(164226-14-6)

Safety Data

• Hazardous Substances Data: 164226-14-6(Hazardous Substances Data)

Upstream product

• 1239374-08-3 tert-butyl 4-isopropylphenyl(3-perfluorooctylpropoxy)carbamate 
• 24424-99-5 di-tert-butyl dicarbonate 
• 99-88-7 4-Isopropylaniline 

Downstream Products

• 628293-26-5 (S)-N-(4-isopropyl)phenyl-N'-(1-methyl-2-hydroxy)ethylurea 
• 628293-18-5 (R)-N-(4-isopropyl)phenyl-N'-(1-methyl-2-hydroxy)ethylurea 
• 628293-19-6 (R)-N-(4-isopropyl)phenyl-N'-(1-ethyl-2-hydroxy)ethylurea 
• 628293-27-6 (S)-N-(4-isopropyl)phenyl-N'-(1-ethyl-2-hydroxy)ethylurea 
• 164226-27-1 2-[3-tert-Butylsulfanyl-1-(4-chloro-benzyl)-5-isopropyl-1H-indol-2-ylsulfanyl]-2-methyl-propionic acid methyl ester 
• 164226-17-9 2-tert-butylthiomethyl-4-isopropyl-N-tert-butoxycarbonylaniline 

Relevant articles and documents

Sustainable and chemoselective N-Boc protection of amines in biodegradable deep eutectic solvent

Abstract: A green and practical approach for the chemoselective N-tert-butyloxycarbonylation of structurally diverse amines with di-tert-butyl dicarbonate (Boc2O) is described. Selective N-Boc protection was achieved in excellent yields in urea-choline chloride deep eutectic solvent (DES) as the most promising environmentally benign and cost-effective solvent under mild reaction condition. DES can protect various aromatic and aliphatic amines using Boc2O in good to excellent yields in short reaction times without any side products. Graphical abstract: [Figure not available: see fulltext.].

PRODUCTION METHOD FOR AMIDATE COMPOUND

A method for producing an amidate compound represented by Formula (3), comprising reacting a urethane compound represented by Formula (1) with a carboxylate compound represented by Formula (2): (in the formulas, A, n, R1, R2, R3, R4, R5, R6, X, and a are as described in the Description).

Amidate compound, catalyst for polyurethane production, and method for producing polyurethane resin

Provided is an amidate compound represented by the formula (1): wherein A is a substituted or unsubstituted hydrocarbon group, n is an integer of 1 or more, and D is a nitrogen-containing organic group represented by the formula (2): wherein R1, R2, and R3 are the same or different, and are each a hydrocarbon group that may contain a heteroatom; some or all of R1, R2, and R3 may be bonded together to form a ring structure; X is a nitrogen atom, an oxygen atom, or a sulfur atom; and a is 0 or 1, wherein a is 1 when X is a nitrogen atom, and a is 0 when X is an oxygen atom or a sulfur atom.