320580-88-9

Basic information

• Product Name: Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI)
• Synonyms: Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI);tert-butyl 2-(isopropylamino)ethylcarbamate;tert-butyl N-{2-[(propan-2-yl)aMino]ethyl}carbaMate;N-[2-[(1-methylethyl)amino]ethyl]carbamic acid tert-butyl ester
• CAS NO: 320580-88-9
• Molecular Formula: C₁₀H₂₂N₂O₂
• Molecular Weight: 202.29388
• Product Categories: N-BOC
• Mol File: 320580-88-9.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 289℃
• Flash Point: 129℃
• Appearance: /
• Density: 0.940
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI)(320580-88-9)
• EPA Substance Registry System: Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI)(320580-88-9)

Safety Data

• Hazardous Substances Data: 320580-88-9(Hazardous Substances Data)

Usage

General Description

Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI) is a chemical compound commonly known as tert-butyl N-(isopropyl)carbamate. It is an ester derivative of carbamic acid and is used in pharmaceutical and agricultural industries. Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI) is primarily used as a synthetic intermediate in the production of various drugs and pesticides. It is also used as a reagent in organic synthesis and as a precursor in the manufacturing of other chemicals. Furthermore, this compound has been studied for its potential use as a chelating agent for metal ions and as a stabilizer in polymer materials. However, it is important to note that this compound may have potential health and safety hazards and should be handled with caution.

Upstream product

• 57260-73-8 N-BOC-1,2-diaminoethane 
• 75-26-3 isopropyl bromide 
• 24424-99-5 di-tert-butyl dicarbonate 
• 96628-67-0 2-(tert-butoxycarbonylamino)ethyl methanesulfonate 
• 75-31-0 isopropylamine 
• 26690-80-2 2-(N-tert-butoxycarbonylamino)ethanol 
• 89711-08-0 N-(t-butoxycarbonyl)glycinal 
• 39684-80-5 2-(tert-butoxycarbonylamino)ethyl bromide 
• 19522-67-9 N-isopropylethane-1,2-diamine 
• 58632-95-4 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile 

Downstream Products

• 19522-67-9 N-isopropylethane-1,2-diamine 
• 1015686-66-4 rac-3-[(2-Amino-ethyl)-isopropyl-amino]-6-chloro-3-(3-chloro-benzyl)-1,3-dihydro-indol-2-one 

Relevant articles and documents

Design, synthesis, and biological evaluation of novel phenol ether derivatives as non-covalent proteasome inhibitors

A series of novel phenol ether derivatives were designed, synthesized, and evaluated as non-covalent proteasome inhibitors. Most compounds exhibited moderate to excellent proteasome inhibitory activity. In particular, compound 18x proved to be the most po

Highly enantioselective synthesis of 2,3-dihydro-1 H-imidazo[2,1-a isoindol-5(9b H)-ones via catalytic asymmetric intramolecular cascade imidization-nucleophilic addition-lactamization

Highly enantioselective catalytic asymmetric intramolecular cascade imidization-nucleophilic addition-lactamization of N1-alkylethane-1,2-diamine with methyl 2-formylbenzoate catalyzed by a chiral phosphoric acid represents the first efficient method for the preparation of medicinally interesting chiral 2,3-dihydro-1H-imidazo[2,1-a]isoindol-5(9bH)-ones with high yields and excellent enantioselectivities. This strategy has been shown to be quite general toward various methyl 2-formylbenzoates.

Preparation of mono Boc-protected unsymmetrical diamines

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