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3-(4-phenylacetic acid)-1,2,4,5-tetrazine succinimidyl ester

Base Information
  • Chemical Name:3-(4-phenylacetic acid)-1,2,4,5-tetrazine succinimidyl ester
  • CAS No.:1616668-55-3
  • Molecular Formula:C14H11N5O4
  • Molecular Weight:313.272
  • Hs Code.:
3-(4-phenylacetic acid)-1,2,4,5-tetrazine succinimidyl ester

Synonyms:3-(4-phenylacetic acid)-1,2,4,5-tetrazine succinimidyl ester

Suppliers and Price of 3-(4-phenylacetic acid)-1,2,4,5-tetrazine succinimidyl ester
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
  • Chem-Impex
  • Tetrazine-NHS ester ≥ 95% (HPLC)
  • 250MG
  • $ 650.00
  • Chem-Impex
  • Tetrazine-NHS ester ≥ 95% (HPLC)
  • 100MG
  • $ 295.00
  • Chem-Impex
  • Tetrazine-NHS ester ≥ 95% (HPLC)
  • 25MG
  • $ 150.00
  • Chem-Impex
  • Tetrazine-NHS ester ≥ 95% (HPLC)
  • 5MG
  • $ 75.00
  • Chem-Impex
  • Tetrazine-NHS ester ≥ 95% (HPLC)
  • 1G
  • $ 1460.00
  • BroadPharm
  • Tetrazine-NHSester 95%
  • 500 MG
  • $ 850.00
Total 6 raw suppliers
Chemical Property of 3-(4-phenylacetic acid)-1,2,4,5-tetrazine succinimidyl ester
Chemical Property:
  • Boiling Point:547.5±60.0 °C(Predicted) 
  • Density:1.53±0.1 g/cm3(Predicted) 
Purity/Quality:

97% *data from raw suppliers

Tetrazine-NHS ester ≥ 95% (HPLC) *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Description Tetrazine-NHS Ester is a NHS activated tetrazine linker. NHS ester is very reactive with amine containing molecule. Methyltetrazine enable fast click reaction with TCO (trans-cycloctene).
Technology Process of 3-(4-phenylacetic acid)-1,2,4,5-tetrazine succinimidyl ester

There total 1 articles about 3-(4-phenylacetic acid)-1,2,4,5-tetrazine succinimidyl ester 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 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; at 20 ℃; for 6h;
DOI:10.1002/open.201402000
Guidance literature:
With N-ethyl-N,N-diisopropylamine; In methanol; at 0 - 20 ℃; for 1h;
DOI:10.1021/acs.inorgchem.1c01274
Guidance literature:
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; at 20 ℃;
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