4-tert-Butylphenyl glycidyl ether, (+)-

Base Information

Chemical Name:4-tert-Butylphenyl glycidyl ether, (+)-
CAS No.:250778-94-0
Molecular Formula:C₁₃H₁₈O₂
Molecular Weight:206.285
Hs Code.:
UNII:NK233DJ6YF
Nikkaji Number:J1.327.035J
Wikidata:Q27284906

Synonyms:250778-94-0;4-tert-Butylphenyl glycidyl ether, (+)-;(2S)-2-[(4-tert-butylphenoxy)methyl]oxirane;S-4-tert-butylphenoxymethyloxirane;NK233DJ6YF;4-tert-Butylphenyl glycidyl ether, (S)-;(2S)-2-(((4-tert-Butylphenyl)oxy)methyl)oxirane;(2S)-2-[[4-(1,1-Dimethylethyl)phenoxy]methyl]oxirane;Oxirane, ((4-(1,1-dimethylethyl)phenoxy)methyl)-, (2S)-;Oxirane, 2-((4-(1,1-dimethylethyl)phenoxy)methyl)-, (2S)-;UNII-NK233DJ6YF;SCHEMBL1244132;HHRACYLRBOUBKM-GFCCVEGCSA-N;(+)-4-tert-butylphenyl glycidyl ether;(S)-2-(4-tert-butyl-phenoxymethyl)oxirane;(S)-2-(4-tert-butylphenoxymethyl)-oxirane;Q27284906;(2s)-(+)-3-[4'-(t-butyl)phenoxy]-1,2-epoxypropane

Suppliers and Price of 4-tert-Butylphenyl glycidyl ether, (+)-

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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Total 1 raw suppliers

Chemical Property of 4-tert-Butylphenyl glycidyl ether, (+)-

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:206.130679813
Heavy Atom Count:15
Complexity:199

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)C1=CC=C(C=C1)OCC2CO2
Isomeric SMILES:CC(C)(C)C1=CC=C(C=C1)OC[C@@H]2CO2

Technology Process of 4-tert-Butylphenyl glycidyl ether, (+)-

There total 6 articles about 4-tert-Butylphenyl glycidyl ether, (+)- 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: 67.0%

: 67843-74-7,24969-06-0,13403-37-7
(S)-epichlorohydrin

: 98-54-4
para-tert-butylphenol

: 250778-94-0
(2S)-(+)-3-[4'-(t-butyl)phenoxy]-1,2-epoxypropane

Guidance literature:: With potassium carbonate; In acetone; at 45 ℃; for 96h;

Reference yield: 54.0%

: 51594-55-9,24969-06-0,13403-37-7
(R)-(-)-epichlorohydrin

: 98-54-4
para-tert-butylphenol

: 250778-94-0
(2S)-(+)-3-[4'-(t-butyl)phenoxy]-1,2-epoxypropane

Guidance literature:: With sodium hydroxide; In water; at 64 ℃; for 8h;
DOI:10.1016/j.bmc.2004.06.039

Reference yield: 48.0%

: 3101-60-8
4-tert-butylphenyl 2,3-epoxypropyl ether

: 250778-94-0
(2S)-(+)-3-[4'-(t-butyl)phenoxy]-1,2-epoxypropane

: (R)-3-(4-(tert-butyl)phenoxy)propane-1,2-diol

Guidance literature:: 4-tert-butylphenyl 2,3-epoxypropyl ether; With C₅₇H₅₄CoN₃O₈; In dichloromethane; at 20 ℃; for 0.25h;

With water; In dichloromethane; at 20 ℃; for 6h; enantioselective reaction; Cooling with ice;
DOI:10.1002/adsc.201700788