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10-Methyl-11-deazahomofolic acid

Base Information Edit
  • Chemical Name:10-Methyl-11-deazahomofolic acid
  • CAS No.:119770-55-7
  • Molecular Formula:C22H24 N6 O6
  • Molecular Weight:468.46256
  • Hs Code.:
  • Mol file:119770-55-7.mol
10-Methyl-11-deazahomofolic acid

Synonyms:10-Methyl-11-deazahomofolic acid

Suppliers and Price of 10-Methyl-11-deazahomofolic acid
Supply Marketing:Edit
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
  • N-[4-[3-(2-AMINO-1,4-DIHYDRO-4-OXO-6-PTERIDINYL)-2-METHYLPROPYL]BENZOYL]-L-GLUTAMIC ACID(9CI) 95.00%
  • 5MG
  • $ 495.21
Total 0 raw suppliers
Chemical Property of 10-Methyl-11-deazahomofolic acid Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:202.24000 
  • Density:1.54g/cm3 
  • LogP:1.49770 
Purity/Quality:

N-[4-[3-(2-AMINO-1,4-DIHYDRO-4-OXO-6-PTERIDINYL)-2-METHYLPROPYL]BENZOYL]-L-GLUTAMIC ACID(9CI) 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 10-Methyl-11-deazahomofolic acid

There total 10 articles about 10-Methyl-11-deazahomofolic acid 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 4-methyl-morpholine; isobutyl chloroformate; In dimethyl sulfoxide; N,N-dimethyl-formamide; for 18h; solid phase coupling;
DOI:10.1021/jm00126a022
Guidance literature:
Multi-step reaction with 8 steps
1: 56 percent / CH2Cl2 / 40 h / Ambient temperature
2: 41 percent / CuBr / tetrahydrofuran / a) -25 deg C, 2 h, b) r.t., 12 h
3: 99 percent / hydroxylamine hydrochloride, pyridine / methanol / 1 h / Heating
4: 83 percent / hydrazine / methanol / 48 h
5: 75 percent / methylmorpholine / methanol / 3 h / Heating
6: 1N HCl, TFA / 60 °C
8: 50 percent / N-methylmorpholine, isobutyl chloroformate / dimethylformamide; dimethylsulfoxide / 18 h / solid phase coupling
With 4-methyl-morpholine; 2-methylmorpholine; pyridine; hydrogenchloride; hydroxylamine hydrochloride; trifluoroacetic acid; copper(I) bromide; hydrazine; isobutyl chloroformate; In tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1021/jm00126a022
Guidance literature:
Multi-step reaction with 4 steps
1: 75 percent / methylmorpholine / methanol / 3 h / Heating
2: 1N HCl, TFA / 60 °C
4: 50 percent / N-methylmorpholine, isobutyl chloroformate / dimethylformamide; dimethylsulfoxide / 18 h / solid phase coupling
With 4-methyl-morpholine; 2-methylmorpholine; hydrogenchloride; trifluoroacetic acid; isobutyl chloroformate; In methanol; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1021/jm00126a022
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