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2-Thia-6-azaspiro[3.3]heptane oxalic acid salt (2:1)

Base Information
  • Chemical Name:2-Thia-6-azaspiro[3.3]heptane oxalic acid salt (2:1)
  • CAS No.:920491-09-4
  • Molecular Formula:C5H9NS
  • Molecular Weight:115.199
  • Hs Code.:2934999090
  • Mol file:920491-09-4.mol
2-Thia-6-azaspiro[3.3]heptane oxalic acid salt (2:1)

Synonyms:2-thia-6-azaspiro[3.3]heptane

Suppliers and Price of 2-Thia-6-azaspiro[3.3]heptane oxalic acid salt (2:1)
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
  • 2-Thia-6-azaspiro[3.3]heptane 95+%
  • 10g
  • $ 3860.00
  • SynQuest Laboratories
  • 2-Thia-6-azaspiro[3.3]heptane
  • 250 mg
  • $ 592.00
  • SynQuest Laboratories
  • 2-Thia-6-azaspiro[3.3]heptane
  • 1 g
  • $ 1708.00
  • SynQuest Laboratories
  • 2-Thia-6-azaspiro[3.3]heptane
  • 500 mg
  • $ 1148.00
  • Matrix Scientific
  • 2-Thia-6-azaspiro[3.3]heptane 95+%
  • 1g
  • $ 3036.00
  • AK Scientific
  • 2-Thia-6-azaspiro[3.3]heptane
  • 1g
  • $ 802.00
Total 10 raw suppliers
Chemical Property of 2-Thia-6-azaspiro[3.3]heptane oxalic acid salt (2:1)
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

2-Thia-6-azaspiro[3.3]heptane 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 2-Thia-6-azaspiro[3.3]heptane is a useful moiety in anticancer medication as because it makes the molecule a better EGFR kinase inhibitor.
Technology Process of 2-Thia-6-azaspiro[3.3]heptane oxalic acid salt (2:1)

There total 5 articles about 2-Thia-6-azaspiro[3.3]heptane oxalic acid salt (2:1) 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 magnesium; In methanol; at 20 ℃; for 3h; Sonication;
Guidance literature:
Multi-step reaction with 5 steps
1: potassium hydroxide / ethanol / 48 h / 25 - 100 °C
2: hydrogen bromide; acetic acid / diethyl ether / 0.5 h / 20 °C
3: carbon tetrabromide; triphenylphosphine / dichloromethane / 0 - 20 °C
4: sodiumsulfide nonahydrate / water; acetonitrile / 4 h / 50 °C
5: magnesium / methanol / 3 h / 20 °C / Sonication
With sodiumsulfide nonahydrate; carbon tetrabromide; hydrogen bromide; magnesium; acetic acid; triphenylphosphine; potassium hydroxide; In methanol; diethyl ether; ethanol; dichloromethane; water; acetonitrile;
Guidance literature:
Multi-step reaction with 4 steps
1: hydrogen bromide; acetic acid / diethyl ether / 0.5 h / 20 °C
2: carbon tetrabromide; triphenylphosphine / dichloromethane / 0 - 20 °C
3: sodiumsulfide nonahydrate / water; acetonitrile / 4 h / 50 °C
4: magnesium / methanol / 3 h / 20 °C / Sonication
With sodiumsulfide nonahydrate; carbon tetrabromide; hydrogen bromide; magnesium; acetic acid; triphenylphosphine; In methanol; diethyl ether; dichloromethane; water; acetonitrile;
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