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3-(tert-butylamino)propane-1,2-diol

CAS No.: 22741-52-2

product details:

Purity: 99%

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  • Molecular Formula: C7H17NO2
  • Molecular Weight: 147.217
  • Vapor Pressure: 0.00155mmHg at 25°C 
  • Refractive Index: 1.465 
  • Boiling Point: 262.4 °C at 760 mmHg 
  • Flash Point: 109.1 °C 
  • PSA: 52.49000 
  • Density: 0.992 g/cm3 
  • LogP: 0.11860 

3-(tert-butylamino)propane-1,2-diol(Cas 22741-52-2) Usage

General Description

3-(tert-butylamino)propane-1,2-diol is a chemical compound with the molecular formula C8H19NO2. It is a tertiary amine with a hydroxyl group on the second carbon of the propane chain. 3-(tert-butylamino)propane-1,2-diol is commonly used as a chiral auxiliary in organic synthesis to control the stereochemistry of reactions. It can also be used as a resolving agent for enantiomeric mixtures. Additionally, 3-(tert-butylamino)propane-1,2-diol has been studied for its potential as a drug delivery agent due to its ability to form stable complexes with a variety of drugs. Overall, this compound has applications in the pharmaceutical industry and organic synthesis.

InChI:InChI=1/C7H17NO2/c1-7(2,3)8-4-6(10)5-9/h6,8-10H,4-5H2,1-3H3

22741-52-2 Relevant articles

Asymmetric hydrolysis of (R, S)-5-acetoxymethyl-3-tert-butyl- oxazolidin-2-one with enzymes and microorganisms

Hamaguchi,Hasegawa,Kawaharada,Watanabe

, p. 2055 - 2059 (1984)

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Ophthalmic compositions and their use for treating elevated intraocular pressure and glaucoma

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, (2008/06/13)

Antiglaucoma compositions that contain e...

propanolamines. 1. Novel β-Blockers with Ultrashort Duration of Action

Kam, Sheung-Tsam,Matier, William L.,Mai, Khuong X.,Barcelon-Yang, Cynthia,Borgman, Robert J.,et al.

, p. 1007 - 1016 (2007/10/02)

Novel propanolamines were synthesized an...

Total Synthesis of (R)-Glycerol Acetonide and the Antiepileptic and Hypotensive Drug (-)-γ-Amino-β-hydroxybutyric Acid (GABOB): Use of Vitamin C as a Chiral Starting Material

Jung, Michael E.,Shaw, Teresa J.

, p. 6304 - 6311 (2007/10/02)

Ascorbic acid (Vitamin C) (9) is shown t...

22741-52-2 Process route

(DL)-2,2-dimethyl-4-((tert-butylamino)methyl)-1,3-dioxolane
74924-01-9

(DL)-2,2-dimethyl-4-((tert-butylamino)methyl)-1,3-dioxolane

1-tert-butylamino-2,3-dihydroxypropane
22741-52-2

1-tert-butylamino-2,3-dihydroxypropane

Conditions
Conditions Yield
With hydrogenchloride; In water; for 3h; Ambient temperature;
33%
D-pyrrolidone-5-carboxylic acid
4042-36-8

D-pyrrolidone-5-carboxylic acid

1-tert-butylamino-2,3-dihydroxypropane
22741-52-2

1-tert-butylamino-2,3-dihydroxypropane

Conditions
Conditions Yield
In acetone;

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