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2-AMINO-N-MESITYLACETAMIDE HYDROCHLORIDE

Base Information
  • Chemical Name:2-AMINO-N-MESITYLACETAMIDE HYDROCHLORIDE
  • CAS No.:92885-79-5
  • Molecular Formula:C11H16 N2 O
  • Molecular Weight:192.261
  • Hs Code.:2924299090
  • Mol file:92885-79-5.mol
2-AMINO-N-MESITYLACETAMIDE HYDROCHLORIDE

Synonyms:N-(Aminoacetyl)mesidine;N-Glycylmesidine

Suppliers and Price of 2-AMINO-N-MESITYLACETAMIDE 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
  • American Custom Chemicals Corporation
  • 2-AMINO-N-MESITYLACETAMIDE 95.00%
  • 5G
  • $ 1548.26
  • American Custom Chemicals Corporation
  • 2-AMINO-N-MESITYLACETAMIDE 95.00%
  • 2.5G
  • $ 1227.82
  • American Custom Chemicals Corporation
  • 2-AMINO-N-MESITYLACETAMIDE 95.00%
  • 1G
  • $ 852.55
Total 3 raw suppliers
Chemical Property of 2-AMINO-N-MESITYLACETAMIDE HYDROCHLORIDE
Chemical Property:
  • Vapor Pressure:0.000172mmHg at 25°C 
  • Boiling Point:329.9°Cat760mmHg 
  • Flash Point:153.3°C 
  • PSA:58.61000 
  • Density:1.098g/cm3 
  • LogP:3.66080 
Purity/Quality:

99% *data from raw suppliers

2-AMINO-N-MESITYLACETAMIDE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 2-AMINO-N-MESITYLACETAMIDE HYDROCHLORIDE

There total 3 articles about 2-AMINO-N-MESITYLACETAMIDE 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 methanol; at 0 - 20 ℃; for 14h; Inert atmosphere; Schlenk technique;
DOI:10.1016/j.molcata.2016.10.004
Guidance literature:
Multi-step reaction with 2 steps
1.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere; Schlenk technique
1.2: 5 h / 0 - 20 °C / Inert atmosphere; Schlenk technique
2.1: hydrogenchloride / methanol / 14 h / 0 - 20 °C / Inert atmosphere; Schlenk technique
With 4-methyl-morpholine; hydrogenchloride; isobutyl chloroformate; In tetrahydrofuran; methanol;
DOI:10.1016/j.molcata.2016.10.004
Guidance literature:
entsprech. α-Halogenanilid 1) PHT=N-K, 2) H2N-NH2;
DOI:10.1021/jm00196a005
upstream raw materials:

2,4,6-trimethylaniline

Downstream raw materials:

N-2,4,6-trimethylphenyl-(1,2-diaminoethane)

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