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

Encyclopedia

6-O-[2,2-dimethyl-8-(tert-butyldiphenylsilyloxy)-octanoyl]-β-D-galactopyranosyl azide

Base Information Edit
  • Chemical Name:6-O-[2,2-dimethyl-8-(tert-butyldiphenylsilyloxy)-octanoyl]-β-D-galactopyranosyl azide
  • CAS No.:545400-08-6
  • Molecular Formula:C32H47N3O7Si
  • Molecular Weight:613.827
  • Hs Code.:
  • Mol file:545400-08-6.mol
6-O-[2,2-dimethyl-8-(tert-butyldiphenylsilyloxy)-octanoyl]-β-D-galactopyranosyl azide

Synonyms:6-O-[2,2-dimethyl-8-(tert-butyldiphenylsilyloxy)-octanoyl]-β-D-galactopyranosyl azide

Suppliers and Price of 6-O-[2,2-dimethyl-8-(tert-butyldiphenylsilyloxy)-octanoyl]-β-D-galactopyranosyl azide
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 0 raw suppliers
Chemical Property of 6-O-[2,2-dimethyl-8-(tert-butyldiphenylsilyloxy)-octanoyl]-β-D-galactopyranosyl azide Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 6-O-[2,2-dimethyl-8-(tert-butyldiphenylsilyloxy)-octanoyl]-β-D-galactopyranosyl azide

There total 6 articles about 6-O-[2,2-dimethyl-8-(tert-butyldiphenylsilyloxy)-octanoyl]-β-D-galactopyranosyl azide 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:
Multi-step reaction with 5 steps
1.1: 88 percent / imidazole / dimethylformamide / 36 h / 20 °C
2.1: 97 percent / tetrabromomethane; triphenylphosphine / CH2Cl2 / 15 h / 0 - 20 °C
3.1: LDA / tetrahydrofuran; hexane / 2 h / -20 - 50 °C
3.2: 78 percent / tetrahydrofuran; hexane / 1 h / 40 °C
4.1: oxalyl chloride / CH2Cl2 / 20 °C
5.1: 15.90 g / pyridine; DMAP / 20 h / 70 °C
With pyridine; 1H-imidazole; dmap; oxalyl dichloride; carbon tetrabromide; triphenylphosphine; lithium diisopropyl amide; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/chem.200400253
Guidance literature:
Multi-step reaction with 4 steps
1.1: 97 percent / tetrabromomethane; triphenylphosphine / CH2Cl2 / 15 h / 0 - 20 °C
2.1: LDA / tetrahydrofuran; hexane / 2 h / -20 - 50 °C
2.2: 78 percent / tetrahydrofuran; hexane / 1 h / 40 °C
3.1: oxalyl chloride / CH2Cl2 / 20 °C
4.1: 15.90 g / pyridine; DMAP / 20 h / 70 °C
With pyridine; dmap; oxalyl dichloride; carbon tetrabromide; triphenylphosphine; lithium diisopropyl amide; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1002/chem.200400253
Post RFQ for Price