Mabdgo

Base Information

Chemical Name:Mabdgo
CAS No.:78138-59-7
Molecular Formula:C₂₁H₂₇NO₆
Molecular Weight:389.448
Hs Code.:
Mol file:78138-59-7.mol

Synonyms:2-methyl-(2-acetamido-4-O-acetyl-6-O-benzyl-3-O-(2-butenyl)-1,2-dideoxy alpha-D-glucopyrano)(2,1-d)-2-oxazoline;MABDGO

Suppliers and Price of Mabdgo

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 Mabdgo

Chemical Property:

Vapor Pressure:3.89E-10mmHg at 25°C
Boiling Point:500.2°C at 760 mmHg
Flash Point:185.7°C
PSA：75.58000
Density:1.22g/cm³
LogP:2.07390
XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:9
Exact Mass:389.18383758
Heavy Atom Count:28
Complexity:571

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC=CCOC1C2C(OC(C1OC(=O)C)COCC3=CC=CC=C3)OC(=N2)C
Isomeric SMILES:C/C=C/CO[C@H]1[C@H]2[C@@H](O[C@H]([C@@H]1OC(=O)C)COCC3=CC=CC=C3)OC(=N2)C

Technology Process of Mabdgo

There total 6 articles about Mabdgo 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: 50.0%

: 78138-58-6
1-propenyl 2-acetamido-4-O-acetyl-6-O-benzyl-3-O-(2-butenyl)-2-deoxy-β-D-glucopyranoside

: 78138-59-7
2-methyl-<2-acetamido-4-O-acetyl-6-O-benzyl-3-O-(2-butenyl)-1,2-dideoxy-α-D-glucopyrano>-<2,1-d>-2-oxazoline

Guidance literature:: With mercury dichloride; mercury(II) oxide; In acetonitrile; for 5h; Ambient temperature;
DOI:10.1016/S0008-6215(00)85253-2

Reference yield:

: 65947-37-7
allyl 2-deoxy-2-acetamido-4,6-O-benzylidene-β-D-glucopyranoside

: 78138-59-7
2-methyl-<2-acetamido-4-O-acetyl-6-O-benzyl-3-O-(2-butenyl)-1,2-dideoxy-α-D-glucopyrano>-<2,1-d>-2-oxazoline

Guidance literature:: Multi-step reaction with 6 steps

1: 90 percent / barium oxide, barium hydroxide octahydrate / dimethylformamide / 0.5 h / Ambient temperature

2: 93 percent / 60 percent acetic acid / 2 h / 80 °C

3: 33 percent / barium oxide, barium hydroxide octahydrate / dimethylformamide / Ambient temperature

4: 15.3 g / pyridine / 3.5 h / 0 °C

5: 61 percent / 1,4-diazabicyclo<2.2.2>octane / chlorotris(triphenylphosphine)rhodium (I) / ethanol; toluene; H₂O / 2 h / Heating

6: 50 percent / mercuric chloride, mercuric oxide / acetonitrile / 5 h / Ambient temperature

With pyridine; 1,4-diaza-bicyclo[2.2.2]octane; barium hydroxide octahydrate; acetic acid; mercury dichloride; mercury(II) oxide; barium(II) oxide; Wilkinson's catalyst; In ethanol; water; N,N-dimethyl-formamide; toluene; acetonitrile;
DOI:10.1016/S0008-6215(00)85253-2

Reference yield:

: 78138-55-3
allyl 2-acetamido-6-O-benzyl-3-O-(2-butenyl)-2-deoxy-β-D-glucopyranoside

: 78138-59-7
2-methyl-<2-acetamido-4-O-acetyl-6-O-benzyl-3-O-(2-butenyl)-1,2-dideoxy-α-D-glucopyrano>-<2,1-d>-2-oxazoline

Guidance literature:: Multi-step reaction with 3 steps

1: 15.3 g / pyridine / 3.5 h / 0 °C

2: 61 percent / 1,4-diazabicyclo<2.2.2>octane / chlorotris(triphenylphosphine)rhodium (I) / ethanol; toluene; H₂O / 2 h / Heating

3: 50 percent / mercuric chloride, mercuric oxide / acetonitrile / 5 h / Ambient temperature

With pyridine; 1,4-diaza-bicyclo[2.2.2]octane; mercury dichloride; mercury(II) oxide; Wilkinson's catalyst; In ethanol; water; toluene; acetonitrile;
DOI:10.1016/S0008-6215(00)85253-2