120157-98-4

Basic information

• Product Name: Carbamic acid, acetyl-, 1,1-dimethylethyl ester (9CI)
• Synonyms: tert-Butyl N-acetylcarbamate;Acetylcarbamic acid 1,1-dimethylethyl ester;tert-Butyl acetylcarbaMate;CarbaMic acid, acetyl-, 1,1-diMethylethyl ester;Carbamic acid, acetyl-, 1,1-dimethylethyl ester (9CI)
• CAS NO: 120157-98-4
• Molecular Formula: C₇H₁₃NO₃
• Molecular Weight: 159.18302
• Product Categories: N-BOC
• Mol File: 120157-98-4.mol
• Article Data: 8

Chemical Properties

• Appearance: White to off-white powder
• Density: 1.036 g/cm³
• Refractive Index: 1.432
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Carbamic acid, acetyl-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, acetyl-, 1,1-dimethylethyl ester (9CI)(120157-98-4)
• EPA Substance Registry System: Carbamic acid, acetyl-, 1,1-dimethylethyl ester (9CI)(120157-98-4)

Safety Data

• Hazardous Substances Data: 120157-98-4(Hazardous Substances Data)

Usage

General Description

Carbamic acid, acetyl-, 1,1-dimethylethyl ester (9CI) is a chemical compound with the molecular formula C6H13NO2. It is more commonly known as tert-butyl acetate and is often used as a solvent in the production of coatings, inks, and adhesives. It is a colorless liquid with a fruity odor and is flammable. Tert-butyl acetate is also used as a flavor and fragrance agent in the food and beverage industry. It is important to handle this chemical with care and follow safety guidelines when working with it, due to its potential flammability and reactivity.

InChI:InChI=1/C7H13NO3/c1-5(9)8-6(10)11-7(2,3)4/h1-4H3,(H,8,9,10)

Upstream product

• 3744-87-4 N-t-butyloxycarbonyl-DL-alanine 
• 4248-19-5 tert-butyl carbazate 
• 108-24-7 acetic anhydride 
• 41840-28-2 S-tert-butoxycarbonyl-4,6-dimethyl-2-mercaptopyrimidine 
• 15761-38-3 L-N-Boc-Ala 
• 38267-76-4 tert-butyl N-ethylcarbamate 

Downstream Products

• 60-35-5 acetamide 
• 91230-14-7 1-<(tert-butoxycarbonyl)amino>-2(E)-hexene 
• 158807-44-4 ((R)-1-Vinyl-butyl)-carbamic acid tert-butyl ester 
• 956101-42-1 C₆H₅C₃H₄NC₂H₃OC₅H₉O₂ 

Relevant articles and documents

New Synthetic Method of Imides through Oxidative Photodecarboxylation Reaction of N-Protected α-Amino Acids with FSM-16

FSM-16, a mesoporous silica, was found to promote the oxidative photodearboxylation of N-acyl-protected α-amino acids in hexane to afford the corresponding imides.

Deuterium-modified carbapenem derivatives

The invention belongs to the technical field of medicines, and particularly relates to deuterium-modified carbapenem derivatives or pharmaceutically acceptable salts thereof, a method for preparing the compounds, pharmaceutical preparations and pharmaceut

Synthesis of N-Acyl carbamates and oxazolidinones using HClO 4-SiO2 as catalyst under solvent-free conditions

Silica supported perchloric acid catalyzes efficiently the reaction of carbamates and oxazolidinones with anhydrides in the presence of silica sulfuric acid under solvent-free conditions. All the reactions were done at room temperature and the N-acyl carb