Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

beta-D-xylo-Hexopyranosiduronic acid, methyl 3-amino-3,4-dideoxy- (9CI)

Base Information Edit
  • Chemical Name:beta-D-xylo-Hexopyranosiduronic acid, methyl 3-amino-3,4-dideoxy- (9CI)
  • CAS No.:116233-66-0
  • Molecular Formula:C7H13NO5
  • Molecular Weight:191.184
  • Hs Code.:
  • Mol file:116233-66-0.mol
beta-D-xylo-Hexopyranosiduronic acid, methyl 3-amino-3,4-dideoxy- (9CI)

Synonyms:beta-D-xylo-Hexopyranosiduronic acid, methyl 3-amino-3,4-dideoxy- (9CI)

Suppliers and Price of beta-D-xylo-Hexopyranosiduronic acid, methyl 3-amino-3,4-dideoxy- (9CI)
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 1 raw suppliers
Chemical Property of beta-D-xylo-Hexopyranosiduronic acid, methyl 3-amino-3,4-dideoxy- (9CI) Edit
Chemical Property:
  • PSA:102.01000 
  • LogP:-0.77910 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of beta-D-xylo-Hexopyranosiduronic acid, methyl 3-amino-3,4-dideoxy- (9CI)

There total 11 articles about beta-D-xylo-Hexopyranosiduronic acid, methyl 3-amino-3,4-dideoxy- (9CI) 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:
Guidance literature:
With potassium hydroxide; In ethanol; for 192h; Heating;
DOI:10.1021/jo00255a020
Guidance literature:
Multi-step reaction with 9 steps
1: oxalyl chloride / toluene / 0.5 h
2: Et3N / toluene / 23 °C
3: pentane / 1 h
4: Br(coll)2ClO4 (bromonium bis(collidine) perchlorate) / CH2Cl2 / 1.) 5 min. -78 deg C; 2.) from -78 deg C to RT
5: 290 mg / potassium tert-butoxide / dimethylsulfoxide / 12 h / 23 °C
6: 92 percent / m-chloroperbenzoic acid (mCPBA) / 12 h / 23 °C
7: 99 percent / 4-(N,N-dimethylamino)pyridine, triethylamine / CH2Cl2 / 3 h / 23 °C
8: 76 percent / CAN, silica gel / acetonitrile; H2O / 0.17 h / 23 °C
9: potassium hydroxide / aq. ethanol / 192 h / Heating
With dmap; potassium hydroxide; oxalyl dichloride; ammonium cerium(IV) nitrate; bromonium bis(collidine) perchlorate; potassium tert-butylate; silica gel; triethylamine; 3-chloro-benzenecarboperoxoic acid; In ethanol; dichloromethane; water; dimethyl sulfoxide; toluene; acetonitrile; pentane;
DOI:10.1021/jo00255a020
Guidance literature:
Multi-step reaction with 10 steps
1: 95 percent / 1 h / 150 °C
2: oxalyl chloride / toluene / 0.5 h
3: Et3N / toluene / 23 °C
4: pentane / 1 h
5: Br(coll)2ClO4 (bromonium bis(collidine) perchlorate) / CH2Cl2 / 1.) 5 min. -78 deg C; 2.) from -78 deg C to RT
6: 290 mg / potassium tert-butoxide / dimethylsulfoxide / 12 h / 23 °C
7: 92 percent / m-chloroperbenzoic acid (mCPBA) / 12 h / 23 °C
8: 99 percent / 4-(N,N-dimethylamino)pyridine, triethylamine / CH2Cl2 / 3 h / 23 °C
9: 76 percent / CAN, silica gel / acetonitrile; H2O / 0.17 h / 23 °C
10: potassium hydroxide / aq. ethanol / 192 h / Heating
With dmap; potassium hydroxide; oxalyl dichloride; ammonium cerium(IV) nitrate; bromonium bis(collidine) perchlorate; potassium tert-butylate; silica gel; triethylamine; 3-chloro-benzenecarboperoxoic acid; In ethanol; dichloromethane; water; dimethyl sulfoxide; toluene; acetonitrile; pentane;
DOI:10.1021/jo00255a020
Refernces Edit
Post RFQ for Price