3-(Morpholine-4-carboxamido)phenyl morpholine-4-carboxylate

Base Information

• Chemical Name: 3-(Morpholine-4-carboxamido)phenyl morpholine-4-carboxylate
• CAS No.: 6543-97-1
• Molecular Formula: C₆H₁₀O₈
• Molecular Weight: 210.141
• DSSTox Substance ID: DTXSID60352810
• Wikidata: Q82130181
• ChEMBL ID: CHEMBL1337733

Synonyms:6543-97-1;SMR000071031;329228-18-4;3-[(morpholine-4-carbonyl)amino]phenyl morpholine-4-carboxylate;3-[(4-morpholinylcarbonyl)amino]phenyl 4-morpholinecarboxylate;MLS000066823;MLS002540683;F1021-1034;CHEMBL1337733;DTXSID60352810;3-(morpholine-4-carboxamido)phenyl morpholine-4-carboxylate;HMS2369J07;AKOS002243163;SR-01000236860;SR-01000236860-1

Chemical Property of 3-(Morpholine-4-carboxamido)phenyl morpholine-4-carboxylate

Chemical Property:

• Vapor Pressure: 2.62E-13mmHg at 25°C
• Boiling Point: 576.9°Cat760mmHg
• Flash Point: 302.7°C
• Density: 1.344g/cm³
• XLogP3: 0.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• Exact Mass: 335.14812078
• Heavy Atom Count: 24
• Complexity: 435

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1COCCN1C(=O)NC2=CC(=CC=C2)OC(=O)N3CCOCC3

Technology Process of 3-(Morpholine-4-carboxamido)phenyl morpholine-4-carboxylate

There total 20 articles about 3-(Morpholine-4-carboxamido)phenyl morpholine-4-carboxylate 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:

(2E,4E)-2,4-hexadienedioic acid (3588-17-8) → meso-galactaric acid (526-99-8,1213827-87-2,7231-46-1) + DL-idaric acid (87-73-0,526-99-8,527-00-4,608-60-6,5627-26-9,5666-23-9,5768-54-7,6543-97-1,7558-19-2,22076-54-6,25525-21-7,33012-63-4,57030-41-8,80876-58-0,117468-78-7,117468-79-8,7231-46-1)

Guidance literature:

With sodium chlorate; osmium(VIII) oxide; acetic acid;

Reference yield:

(2E,4E)-2,4-hexadienedioic acid (3588-17-8) + acetic acid (64-19-7,77671-22-8) → DL-tartaric acid (133-37-9,138508-61-9) + meso-galactaric acid (526-99-8,1213827-87-2,7231-46-1) + DL-idaric acid (87-73-0,526-99-8,527-00-4,608-60-6,5627-26-9,5666-23-9,5768-54-7,6543-97-1,7558-19-2,22076-54-6,25525-21-7,33012-63-4,57030-41-8,80876-58-0,117468-78-7,117468-79-8,7231-46-1) + oxalic acid (144-62-7,97993-78-7)

Guidance literature:

Reference yield:

D-myo-inositol (87-89-8) → allo-mucic acid (527-00-4,7231-46-1) + DL-glucaric acid (87-73-0,526-99-8,527-00-4,608-60-6,5627-26-9,5666-23-9,5768-54-7,6543-97-1,7558-19-2,22076-54-6,25525-21-7,33012-63-4,57030-41-8,80876-58-0,117468-78-7,117468-79-8,7231-46-1) + oxalic acid (144-62-7,97993-78-7)

Guidance literature:

upstream raw materials:

gluconic acid

inositol

nitric acid

D-myo-inositol

Downstream raw materials:

idaric acid bis-(N'-phenyl-hydrazide)

L-idaric acid

galactaric acid

DL-altruronic acid

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