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(S)-4-(4-Hydrazinylbenzyl)-2-oxazolidinone

Base Information
  • Chemical Name:(S)-4-(4-Hydrazinylbenzyl)-2-oxazolidinone
  • CAS No.:187975-62-8
  • Molecular Formula:C10H13N3O2
  • Molecular Weight:207.232
  • Hs Code.:
  • Mol file:187975-62-8.mol
(S)-4-(4-Hydrazinylbenzyl)-2-oxazolidinone

Synonyms:(S)-4-(4-Hydrazinylbenzyl)-2-oxazolidinone;(4S)-4-[(4-hydrazinylphenyl)Methyl]-2-Oxazolidinone;Zolmitriptan Impurity 1

Suppliers and Price of (S)-4-(4-Hydrazinylbenzyl)-2-oxazolidinone
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
  • TRC
  • (S)-4-(4-Hydrazinylbenzyl)-2-oxazolidinone
  • 250mg
  • $ 1320.00
  • Crysdot
  • (S)-4-(4-Hydrazinylbenzyl)oxazolidin-2-one 95+%
  • 1g
  • $ 972.00
  • Chemenu
  • (S)-4-(4-hydrazinylbenzyl)oxazolidin-2-one 95%
  • 1g
  • $ 916.00
Total 8 raw suppliers
Chemical Property of (S)-4-(4-Hydrazinylbenzyl)-2-oxazolidinone
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:519.346°C at 760 mmHg 
  • Flash Point:267.891°C 
  • PSA:76.38000 
  • Density:1.318g/cm3 
  • LogP:1.72520 
  • Storage Temp.:Refrigerator 
  • Solubility.:Dimethylformamide 
Purity/Quality:

97% *data from raw suppliers

(S)-4-(4-Hydrazinylbenzyl)-2-oxazolidinone *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses An intermediate of Zolmitriptan, as a novel inhibitor of the cytochrome P-450 enzyme aromatase.
Technology Process of (S)-4-(4-Hydrazinylbenzyl)-2-oxazolidinone

There total 2 articles about (S)-4-(4-Hydrazinylbenzyl)-2-oxazolidinone 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:
(S)-4-(4-aminobenzyl)-1,3-oxazolidin-2-one; With sodium nitrite; In water; at -5 - 0 ℃; for 0.75h;
With triphenylphosphine; In methanol; diethyl ether; water; at 5 - 20 ℃; for 8h;
Guidance literature:
4-((S)-2-Oxo-oxazolidin-4-ylmethyl)-benzenediazonium; chloride; With hydrogenchloride; tin(ll) chloride; In water; at -10 - 5 ℃; for 4h; pH=~ 2;
With sodium carbonate; In water; at 25 - 30 ℃; pH=8 - 9;
Guidance literature:
4-aminobutyrylaldehyde diethylacetal; (S)-4-(4-hydrazinobenzyl)-1,3-oxazolidin-2-one; With hydrogenchloride; In water; at 90 ℃; for 1h;
With sodium hydroxide; In water; pH=7;
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