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6-AMINOHEXYL 1-THIO-B-D-GALACTOPYRANOSID E

Base Information Edit
  • Chemical Name:6-AMINOHEXYL 1-THIO-B-D-GALACTOPYRANOSID E
  • CAS No.:51224-14-7
  • Molecular Formula:C12H25NO5S
  • Molecular Weight:295.3956
  • Hs Code.:
  • Mol file:51224-14-7.mol
6-AMINOHEXYL 1-THIO-B-D-GALACTOPYRANOSID E

Synonyms:6-AMINOHEXYL 1-THIO-B-D-GALACTOPYRANOSID E;6-aminohexyl-1-thio-beta-D-galactopyranoside

Suppliers and Price of 6-AMINOHEXYL 1-THIO-B-D-GALACTOPYRANOSID E
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
  • American Custom Chemicals Corporation
  • 6-AMINOHEXYL-1-THIO-BETA-D-GALACTOPYRANOSID E 95.00%
  • 5MG
  • $ 500.74
Total 2 raw suppliers
Chemical Property of 6-AMINOHEXYL 1-THIO-B-D-GALACTOPYRANOSID E Edit
Chemical Property:
  • PSA:141.47000 
  • LogP:-0.26110 
Purity/Quality:

99%, *data from raw suppliers

6-AMINOHEXYL-1-THIO-BETA-D-GALACTOPYRANOSID E 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 6-AMINOHEXYL 1-THIO-B-D-GALACTOPYRANOSID E

There total 5 articles about 6-AMINOHEXYL 1-THIO-B-D-GALACTOPYRANOSID E 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 4 steps
1: 70 percent / 1.) room temp., 5 h, 2.) 4 deg C
2: method in ref. 1
3: method in ref. 1
DOI:10.1016/S0008-6215(00)85209-X
Guidance literature:
Multi-step reaction with 3 steps
1: method in ref. 1
2: method in ref. 1
DOI:10.1016/S0008-6215(00)85209-X
Refernces Edit
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