N-[5-(1,2-dihydroxyethyl)-4-hydroxy-2-oxooxolan-3-yl]acetamide

Base Information

• Chemical Name: N-[5-(1,2-dihydroxyethyl)-4-hydroxy-2-oxooxolan-3-yl]acetamide
• CAS No.: 28876-37-1
• Molecular Formula: C8H13 N O6
• Molecular Weight: 219.1919
• NSC Number: 297283,25295
• Mol file: 28876-37-1.mol

Synonyms:N-[5-(1,2-dihydroxyethyl)-4-hydroxy-2-oxooxolan-3-yl]acetamide;28876-37-1;28876-38-2;N-[5-(1,2-DIHYDROXYETHYL)-4-HYDROXY-2-OXO-OXOLAN-3-YL]ACETAMIDE;686299-03-6;2-Acetamido-2-deoxy-D-mannono-1,4-lactone;D-Mannonic acid, 2-(acetylamino)-2-deoxy-, gamma-lactone;D-Galactonic acid, 2-(acetylamino)-2-deoxy-, gamma-lactone;N-(5-(1,2-Dihydroxyethyl)-4-hydroxy-2-oxotetrahydrofuran-3-yl)acetamide;NSC25295;SCHEMBL6675908;JYOPKUOOYNIILV-UHFFFAOYSA-N;NSC-25295;NSC297283;AB07119;NSC-297283;2-Acetamide-2-deoxygalactono-1,4-lactone;FT-0660990;FT-0661009;2-ACETAMIDO-2-DEOXY-D-GALACTONICACID1,4-LACTONE

Chemical Property of N-[5-(1,2-dihydroxyethyl)-4-hydroxy-2-oxooxolan-3-yl]acetamide

Chemical Property:

• Melting Point: 172-173°C
• Boiling Point: 681.8 ºC at 760 mmHg
• PKA: 11.97±0.60(Predicted)
• Flash Point: 366.1 ºC
• PSA: 116.09000
• Density: 1.5 g/cm3
• LogP: -2.47850
• Storage Temp.: -20°C Freezer
• XLogP3: -2
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 219.07428713
• Heavy Atom Count: 15
• Complexity: 268

Purity/Quality:

98%min ^*data from raw suppliers

2-Acetamido-2-deoxy-D-mannono-1,4-lactone ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)NC1C(C(OC1=O)C(CO)O)O

Technology Process of N-[5-(1,2-dihydroxyethyl)-4-hydroxy-2-oxooxolan-3-yl]acetamide

There total 4 articles about N-[5-(1,2-dihydroxyethyl)-4-hydroxy-2-oxooxolan-3-yl]acetamide 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: 65.0%

2-acetamido-2-deoxy-D-galactose N,N'-diphenylformazan (87924-40-1,87924-41-2,87924-43-4) → 2-Acetamido-2-desoxy-D-galactono-1,4-lacton (5469-77-2,28876-37-1,28876-38-2)

Guidance literature:

With trifluoroacetic acid; In methanol; ethanol; Ambient temperature;

DOI:10.1016/0008-6215(94)90007-8

Reference yield: 41.0%

N-acetyl-D-mannosamine (72-87-7,1136-42-1,1136-44-3,6082-29-7,6730-06-9,7772-94-3,10036-64-3,14131-60-3,14131-64-7,14131-68-1,14215-68-0,62057-49-2,62057-50-5,62057-51-6,62057-52-7,62057-53-8,62057-54-9,62057-55-0,62057-56-1,62075-50-7,62137-54-6,134451-97-1,134522-12-6,148347-16-4) → 2-acetamido-2-deoxy-D-mannono-1,4-lactone (28876-37-1)

Guidance literature:

With bromine; In water;

DOI:10.1016/0040-4039(94)88467-6

Reference yield:

→ 2-acetamido-2-deoxy-D-mannono-1,4-lactone (28876-37-1)

Guidance literature:

a) Verb. 2, Brom;

DOI:10.1016/S0008-6215(00)86164-9

upstream raw materials:

2-acetamido-2-deoxy-D-galactose N,N'-diphenylformazan

N-acetyl-D-mannosamine

Downstream raw materials:

2-acetamido-2-deoxy-D-galacticol

2-acetamido-2-deoxy-5,6-O-benzylidene-D-mannono-1,4-lactone

2-acetamido-5,6-O-benzylidene-3-O-(tert-butyldimethylsilyl)-2-deoxy-D-mannono-1,4-lactone

2-acetamido-6-O-acetyl-2,3-didehydro-2,3-dideoxy-D-erythro-hexono-1,4-lactone