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

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

Uses

Used in Coatings Industry:
Tert-butyl acetate is used as a solvent in the production of coatings, contributing to the desired properties of the final product, such as drying time, adhesion, and gloss.
Used in Inks Industry:
In the inks industry, tert-butyl acetate is utilized as a solvent to improve the flow and drying characteristics of inks, ensuring consistent application and appearance on various surfaces.
Used in Adhesives Industry:
Tert-butyl acetate serves as a solvent in the formulation of adhesives, enhancing their bonding properties and facilitating better adhesion to different substrates.
Used in Food and Beverage Industry:
As a flavor and fragrance agent, tert-butyl acetate is used in the food and beverage industry to impart specific tastes and aromas to products, enhancing their overall sensory appeal.
Safety Precautions:
It is crucial to handle tert-butyl acetate with care and follow safety guidelines when working with it, due to its potential flammability and reactivity. Proper storage, handling, and disposal practices should be implemented to minimize risks associated with its use.

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

Upstream product

• 38267-76-4 tert-butyl N-ethylcarbamate 
• 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 

Downstream Products

• 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 
• 60-35-5 acetamide 

Relevant articles and documents

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PROBLEM TO BE SOLVED: To provide a salt of an isolated compound containing an amide group, a method for producing the same, and a method for synthesizing an amide compound using the same. SOLUTION: The present invention provides a salt of an isolated compound containing an amide group represented by formula (1) (M is an element belonging to group 1 in the periodic table; P is a first protective group of an amine represented by R1-O(C=O)-; Q is a second protective group of an amine represented by R2-(C=O)-; R1 and R2 independently represent a substituted/unsubstituted hydrocarbon group). SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

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