Hydroxyethyl

Base Information

• Chemical Name: Hydroxyethyl
• CAS No.: 2348-46-1
• Molecular Formula: C2H5 O
• Molecular Weight: 45.0611
• DSSTox Substance ID: DTXSID10946162
• Nikkaji Number: J502.841H
• Mol file: 2348-46-1.mol

Synonyms:1-Hydroxyethyl;Ethyl, 1-hydroxy-;2348-46-1;Hydroxyethyl;CH3CHOH;Ethyl radical, 1-hydroxy;C2H5O;DTXSID10946162

Chemical Property of Hydroxyethyl

Chemical Property:

• PSA: 20.23000
• LogP: -0.12600
• XLogP3: -0.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 45.034039779
• Heavy Atom Count: 3
• Complexity: 2.8

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C[CH]O

Technology Process of Hydroxyethyl

There total 6 articles about Hydroxyethyl which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

α-hydroxybenzyl radical (2406-15-7) + acetaldehyde (75-07-0,9002-91-9) → ethanol radical (2348-46-1) + benzaldehyde (100-52-7)

Guidance literature:

Thermodynamic data; Mechanism; ΔE(excit.), ΔH, other ketyl radicals, other carbonyl compounds;

DOI:10.1007/BF02494263

Reference yield:

ethanol (64-17-5) + Penicillamine thiyl radical (58167-41-2) → ethanol radical (2348-46-1) + L-penicillamine (1113-41-3)

Guidance literature:

With perchloric acid; In water; Rate constant; Ambient temperature;

DOI:10.1039/ft9959101923

Reference yield:

hydroquinone radical (3225-30-7) + acetaldehyde (75-07-0,9002-91-9) → ethanol radical (2348-46-1) + p-benzoquinone (106-51-4)

Guidance literature:

Thermodynamic data; Mechanism; ΔE(excit.), ΔH, other ketyl radicals, other carbonyl compounds;

DOI:10.1007/BF02494263

upstream raw materials:

ethanol

Penicillamine thiyl radical

α-hydroxybenzyl radical

acetaldehyde

Downstream raw materials:

acetaldehyde

4-nitrobenzaldehyde radical anion

1-(4-nitro-phenyl)-ethanone; radical anion

4-Nitrobenzonitrile radical anion

Refernces

• 1、 Denisov. "The reactivity of ketyl and alkyl radicals in reactions with carbonyl compounds". . p. 2110 - 2116. Retrieved 2007/10/03.