(s)-1-Chloro-3-phenoxy-2-propanol

Base Information

Chemical Name:(s)-1-Chloro-3-phenoxy-2-propanol
CAS No.:82430-43-1
Molecular Formula:C9H11ClO2
Molecular Weight:186.638
Hs Code.:
DSSTox Substance ID:DTXSID10471666
Nikkaji Number:J1.079.303C
Wikidata:Q82300299

Synonyms:(s)-1-chloro-3-phenoxy-2-propanol;82430-43-1;SCHEMBL6306513;DTXSID10471666;HCTDRZMGZRHFJV-MRVPVSSYSA-N;(2S)-1-CHLORO-3-PHENOXYPROPAN-2-OL

Suppliers and Price of (s)-1-Chloro-3-phenoxy-2-propanol

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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Total 0 raw suppliers

Chemical Property of (s)-1-Chloro-3-phenoxy-2-propanol

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:186.0447573
Heavy Atom Count:12
Complexity:113

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)OCC(CCl)O
Isomeric SMILES:C1=CC=C(C=C1)OC[C@@H](CCl)O

Technology Process of (s)-1-Chloro-3-phenoxy-2-propanol

There total 26 articles about (s)-1-Chloro-3-phenoxy-2-propanol 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: 84.0%

: 106-89-8,24969-06-0,13403-37-7
epichlorohydrin

: 108-95-2,27073-41-2
phenol

: 82430-43-1
(S)-3-chloro-1-phenoxy-2-propanol

Guidance literature:: With chiral (salen)Co-BF₃ complex immobilized on Mesoporous silica (SBA-16 foam); In tert-butyl methyl ether; at 20 ℃; for 7h; under 15201 Torr; Solvent; enantioselective reaction; Flow reactor;
DOI:10.1002/bkcs.10271

Reference yield: 41.0%

: 140428-46-2
1-chloro-3-phenoxypropan-2-yl acetate

: 82430-43-1
(S)-3-chloro-1-phenoxy-2-propanol

: 140630-45-1
(R)-1-chloro-3-phenoxy-2-propanol

: 140924-05-6
(R)-2-acetoxy-1-phenoxy-3-chloropropane

Guidance literature:: With sodium hydroxide; phosphate buffer; at 20 ℃; Yield given. Yields of byproduct given. Title compound not separated from byproducts; pH 7.0, lipase from Pseudomonas sp.;
DOI:10.1016/S0957-4166(00)80191-3

Reference yield: 27.8%

: 4769-73-7
(RS)-1-chloro-3-phenyloxy-2-propanol

: 82430-43-1
(S)-3-chloro-1-phenoxy-2-propanol

: 140630-37-1
(2R)-1-azido-3-phenoxypropan-2-ol

: 140630-41-7
(S)-1-azido-3-phenoxy-2-propanol

Guidance literature:: With sodium azide; recombinant alphaproteobacterium halohydrin dehalogenase; In ethanol; at 30 ℃; for 0.366667h; pH=7.5; Concentration; Time; pH-value; enantioselective reaction; Resolution of racemate; Green chemistry; Enzymatic reaction;
DOI:10.1007/s10562-019-02659-0