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(S)-6-aza-spiro[2.5]octan-4-ol hydrochloride

Base Information
  • Chemical Name:(S)-6-aza-spiro[2.5]octan-4-ol hydrochloride
  • CAS No.:1103501-89-8
  • Molecular Formula:C7H13NO*ClH
  • Molecular Weight:163.647
  • Hs Code.:
(S)-6-aza-spiro[2.5]octan-4-ol hydrochloride

Synonyms:(S)-6-aza-spiro[2.5]octan-4-ol hydrochloride

Suppliers and Price of (S)-6-aza-spiro[2.5]octan-4-ol hydrochloride
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
  • Packaging
  • price
  • Synthonix
  • (4S)-6-Azaspiro[2.5]octan-4-olhydrochloride 95+%
  • 1g
  • $ 1730.00
  • Crysdot
  • (S)-6-Azaspiro[2.5]octan-4-olhydrochloride 95+%
  • 1g
  • $ 1695.00
  • Chemenu
  • (S)-6-Azaspiro[2.5]octan-4-olhydrochloride 95%
  • 1g
  • $ 1597.00
Total 4 raw suppliers
Chemical Property of (S)-6-aza-spiro[2.5]octan-4-ol hydrochloride
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

(4S)-6-Azaspiro[2.5]octan-4-olhydrochloride 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of (S)-6-aza-spiro[2.5]octan-4-ol hydrochloride

There total 10 articles about (S)-6-aza-spiro[2.5]octan-4-ol hydrochloride 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 hydrogenchloride; In 1,4-dioxane; ethanol; at 20 ℃; for 1h;
Guidance literature:
(S)-6-Benzyl-6-aza-spiro[2.5]octan-4-ol; With hydrogen; Pd-BaSO4; In methanol;
With di-tert-butyl dicarbonate; triethylamine; In methanol;
With hydrogenchloride; In ethyl acetate; Product distribution / selectivity;
Guidance literature:
Multi-step reaction with 4 steps
1.1: diethylzinc / toluene; 1,2-dichloro-ethane / 0.25 h / 0 °C / Inert atmosphere
1.2: 0.5 h / 0 °C / Inert atmosphere
2.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -70 - -60 °C
2.2: 0.17 h / -60 °C
3.1: sodium hydroxide; magnesium(II) chloride hexahydrate; α-D-glucose monohydrate / ketoreductase KRED-NADH-117; glucose dehydrogenase GDH-102 / 35 °C / pH 6.5 / Aqueous buffer
4.1: hydrogenchloride / 1,4-dioxane; ethanol / 1 h / 20 °C
With hydrogenchloride; oxalyl dichloride; magnesium(II) chloride hexahydrate; diethylzinc; α-D-glucose monohydrate; dimethyl sulfoxide; sodium hydroxide; ketoreductase KRED-NADH-117; glucose dehydrogenase GDH-102; In 1,4-dioxane; ethanol; dichloromethane; 1,2-dichloro-ethane; toluene; 2.1: Swern Oxidation / 2.2: Swern Oxidation;
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