30533-50-7

Basic information

• Product Name: 1-AMINO-2-METHYL-PROPAN-2-OL HCL
• Synonyms: 1-AMINO-2-METHYL-PROPAN-2-OL HCL;1-Amino-2-methyl-propan-2-ol hydrochloride;2-Propanol, 1-aMino-2-Methyl-, hydrochloride;AMino-2-Methyl-propan-2-ol hydrochloride;EOS-62274
• CAS NO: 30533-50-7
• Molecular Formula: C₄H₁₁NO*ClH
• Molecular Weight: 125.6
• EINECS: 211-923-5
• Mol File: 30533-50-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 210.1°Cat760mmHg
• Flash Point: 80.8°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 0.0448mmHg at 25°C
• CAS DataBase Reference: 1-AMINO-2-METHYL-PROPAN-2-OL HCL(CAS DataBase Reference)
• NIST Chemistry Reference: 1-AMINO-2-METHYL-PROPAN-2-OL HCL(30533-50-7)
• EPA Substance Registry System: 1-AMINO-2-METHYL-PROPAN-2-OL HCL(30533-50-7)

Safety Data

• Hazardous Substances Data: 30533-50-7(Hazardous Substances Data)

Usage

Uses

1-Amino-2-methylpropan-2-ol, HCl

InChI:InChI=1/C4H11NO.ClH/c1-4(2,6)3-5;/h6H,3,5H2,1-2H3;1H

Upstream product

• 85894-38-8 N-Nitroso-N-(2-hydroxy-2-methylpropyl)-1-methoxyethylamine 

Downstream Products

• 558-42-9 3-chloro-2-methylpropan-2-ol 
• 78-84-2 isobutyraldehyde 

Relevant articles and documents

BENZIMIDAZOLONE DERIVATIVES

This invention relates to compounds and methods for the treatment of a condition mediated by CB1 receptor activity in a mammalian subject including a human, which comprises administering to a mammal in need of such treatment a therapeutically effective am

Lithiation of α-Nitrosaminoalkyl Ethers. Synthetic Equivalents of α-Primary Amino Carbanions

Successful experiments directed toward the C-1 alkylation and hydroxyalkylation of primary amines are reported.Primary amines are converted into their N-nitroso-N-(1-methoxyethyl) derivatives, which are subsequently lithiated and condensed with various electrophiles, denitrosated, and hydrolyzed to produce the desired compounds in good to excellent yields.