(1S)-1-Hydroxy-1-phenylheptan-3-one

Base Information

Chemical Name:(1S)-1-Hydroxy-1-phenylheptan-3-one
CAS No.:202744-51-2
Molecular Formula:C13H18O2
Molecular Weight:206.285
Hs Code.:
DSSTox Substance ID:DTXSID00556097
Nikkaji Number:J945.497G
Wikidata:Q82437573

Synonyms:(1S)-1-HYDROXY-1-PHENYLHEPTAN-3-ONE;202744-51-2;DTXSID00556097

Suppliers and Price of (1S)-1-Hydroxy-1-phenylheptan-3-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of (1S)-1-Hydroxy-1-phenylheptan-3-one

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:6
Exact Mass:206.130679813
Heavy Atom Count:15
Complexity:183

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCC(=O)CC(C1=CC=CC=C1)O
Isomeric SMILES:CCCCC(=O)C[C@@H](C1=CC=CC=C1)O

Technology Process of (1S)-1-Hydroxy-1-phenylheptan-3-one

There total 4 articles about (1S)-1-Hydroxy-1-phenylheptan-3-one 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: 98.0%

: 109-72-8,29786-93-4
n-butyllithium

: 264277-66-9
(3S)-3-hydroxy-N-methoxy-N-methyl-3-phenylpropanamide

: 202744-51-2
(-)-(S)-1-hydroxy-1-phenyl-3-heptanone

Guidance literature:: In tetrahydrofuran; at -78 ℃;
DOI:10.1002/ejoc.200900316

Reference yield: 92.3%

: 100-52-7
benzaldehyde

: 202744-35-2
trichloro<(1-butylethenyl)oxy>silane

: 145624-53-9
(+)-(R)-1-hydroxy-1-phenyl-3-heptanone

: 202744-51-2
(-)-(S)-1-hydroxy-1-phenyl-3-heptanone

Guidance literature:: With (S,S)-N,N'-dimethylstilbene-1,2-diamine chiral phosphoramide; In dichloromethane; at -78 ℃; for 2h; Title compound not separated from byproducts.;
DOI:10.1021/ja001023g

Reference yield:

: 60585-82-2
2-trimethylsilyloxy-1-hexene

: 100-52-7
benzaldehyde

: 145624-53-9
(+)-(R)-1-hydroxy-1-phenyl-3-heptanone

: 202744-51-2
(-)-(S)-1-hydroxy-1-phenyl-3-heptanone

Guidance literature:: With hydrogenchloride; 1.) chiral oxazaborolidine 1; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; 1.) propionitrile, -78 deg C, 14 h, 2.) THF, 30 min;
DOI:10.1016/S0040-4039(00)60892-4