4-[6-(3-Phenoxyphenoxy)hexyl]morpholine

Base Information

Chemical Name:4-[6-(3-Phenoxyphenoxy)hexyl]morpholine
CAS No.:5361-88-6
Molecular Formula:C₁₈H₂₅NO₁₀
Molecular Weight:415.397
Hs Code.:
DSSTox Substance ID:DTXSID20368614
Wikidata:Q82155292

Synonyms:5361-88-6;CBMicro_019208;4-[6-(3-phenoxyphenoxy)hexyl]morpholine;DTXSID20368614;CCG-7381;AKOS001038833;BIM-0019326.P001

Suppliers and Price of 4-[6-(3-Phenoxyphenoxy)hexyl]morpholine

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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price

Total 0 raw suppliers

Chemical Property of 4-[6-(3-Phenoxyphenoxy)hexyl]morpholine

Chemical Property:

Vapor Pressure:1.2E-09mmHg at 25°C
Boiling Point:487.4°Cat760mmHg
Flash Point:136.6°C
Density:1.073g/cm³
XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:10
Exact Mass:355.21474379
Heavy Atom Count:26
Complexity:353

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COCCN1CCCCCCOC2=CC(=CC=C2)OC3=CC=CC=C3

Technology Process of 4-[6-(3-Phenoxyphenoxy)hexyl]morpholine

There total 8 articles about 4-[6-(3-Phenoxyphenoxy)hexyl]morpholine 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: 18.0%

: Cellobiose

: 1676-81-9
N-benzyloxycarbonyl-L-serine methyl ester

: 2280-44-6
D-Glucose

: 5361-88-6,5611-37-0,93983-60-9,134308-87-5
N-(benzyloxycarbonyl)-3-O-(β-D-glucopyranosyl)-L-serine methyl ester

Guidance literature:: With β-galactosidase from E. coli; Na phosphate buffer; In water; butanone; at 37 ℃; for 15h; Product distribution; other reagents;
DOI:10.1080/07328309908543986

Reference yield:

: 1145-80-8
N-(benzyloxycarbonyl)-L-serine

: 5361-88-6,5611-37-0,93983-60-9,134308-87-5
N-(benzyloxycarbonyl)-3-O-(β-D-glucopyranosyl)-L-serine methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 75 percent / thionyl chloride / 3 h / 0 °C

2: 46 percent / TMSOTf; 4 Angstroem molecular sieves / CH₂Cl₂ / 3 h

3: 33 percent / hydrazine monohydrate / methanol / 40 h

With thionyl chloride; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; hydrazine hydrate; In methanol; dichloromethane;
DOI:10.1039/b412030b

Reference yield:

: 1676-81-9
N-benzyloxycarbonyl-L-serine methyl ester

: 5361-88-6,5611-37-0,93983-60-9,134308-87-5
N-(benzyloxycarbonyl)-3-O-(β-D-glucopyranosyl)-L-serine methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 46 percent / TMSOTf; 4 Angstroem molecular sieves / CH₂Cl₂ / 3 h

2: 33 percent / hydrazine monohydrate / methanol / 40 h

With trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; hydrazine hydrate; In methanol; dichloromethane;
DOI:10.1039/b412030b