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1',2',3',4',5',6'-hexahydrohomofolic acid

Base Information Edit
  • Chemical Name:1',2',3',4',5',6'-hexahydrohomofolic acid
  • CAS No.:83704-88-5
  • Molecular Formula:C20H27 N7 O6
  • Molecular Weight:461.47168
  • Hs Code.:
  • Mol file:83704-88-5.mol
1',2',3',4',5',6'-hexahydrohomofolic acid

Synonyms:1’,2’,3’,4’,5’,6’-hexahydrohomofolic acid

Suppliers and Price of 1',2',3',4',5',6'-hexahydrohomofolic acid
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 3 raw suppliers
Chemical Property of 1',2',3',4',5',6'-hexahydrohomofolic acid Edit
Chemical Property:
  • PSA:213.28000 
  • Density:1.66g/cm3 
  • LogP:0.78340 
Purity/Quality:
Safty Information:
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  • Hazard Codes: 
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Technology Process of 1',2',3',4',5',6'-hexahydrohomofolic acid

There total 18 articles about 1',2',3',4',5',6'-hexahydrohomofolic 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:
Multi-step reaction with 18 steps
1: 100 percent / H2 / PtO2 / acetic acid / 18 h / 2327.2 Torr
2: 90 percent / 18 h / Ambient temperature
3: thionyl chloride / benzene / 1 h / Heating
4: diethyl ether / 1 h / 25 °C
5: HBr / diethyl ether
6: 91 percent / sodium azide / methanol; H2O / 3.5 h / Ambient temperature
7: p-toluenesulfonic acid / benzene / 6 h / Heating
8: H2 / 10percent Pd/C / 18 h / 517.1 Torr
9: 2.) N-methylmorpholine / 1.) methanol, reflux, 1 h, 2.) methanol, reflux, 3 h
10: 94 percent / trifluoroacetic acid, 0.1 N HCl / 55 - 60 °C
11: 70 percent / sodium ditionite / dimethylformamide; H2O / 0.33 h / 55 °C
12: pyridine, concd. HCl / methanol / 1 h / Heating
13: air / methanol / 4 h
14: 550 mg / 0.1 M NaOH / acetonitrile / 6 h / 25 °C
15: 93 percent / trifluoroacetic acid / 6 h
16: N-methylmorpholine / dimethylformamide / 0.58 h
17: N-methylmorpholine / dimethylformamide / 18 h / 25 °C
18: 0.1 N NaOH / acetonitrile / 6 h / 25 °C
With 4-methyl-morpholine; pyridine; hydrogenchloride; sodium hydroxide; thionyl chloride; sodium azide; sodium dithionite; air; hydrogen bromide; hydrogen; toluene-4-sulfonic acid; trifluoroacetic acid; platinum(IV) oxide; palladium on activated charcoal; In methanol; diethyl ether; water; acetic acid; N,N-dimethyl-formamide; acetonitrile; benzene;
DOI:10.1021/jm00356a004
Guidance literature:
Multi-step reaction with 17 steps
1: 90 percent / 18 h / Ambient temperature
2: thionyl chloride / benzene / 1 h / Heating
3: diethyl ether / 1 h / 25 °C
4: HBr / diethyl ether
5: 91 percent / sodium azide / methanol; H2O / 3.5 h / Ambient temperature
6: p-toluenesulfonic acid / benzene / 6 h / Heating
7: H2 / 10percent Pd/C / 18 h / 517.1 Torr
8: 2.) N-methylmorpholine / 1.) methanol, reflux, 1 h, 2.) methanol, reflux, 3 h
9: 94 percent / trifluoroacetic acid, 0.1 N HCl / 55 - 60 °C
10: 70 percent / sodium ditionite / dimethylformamide; H2O / 0.33 h / 55 °C
11: pyridine, concd. HCl / methanol / 1 h / Heating
12: air / methanol / 4 h
13: 550 mg / 0.1 M NaOH / acetonitrile / 6 h / 25 °C
14: 93 percent / trifluoroacetic acid / 6 h
15: N-methylmorpholine / dimethylformamide / 0.58 h
16: N-methylmorpholine / dimethylformamide / 18 h / 25 °C
17: 0.1 N NaOH / acetonitrile / 6 h / 25 °C
With 4-methyl-morpholine; pyridine; hydrogenchloride; sodium hydroxide; thionyl chloride; sodium azide; sodium dithionite; air; hydrogen bromide; hydrogen; toluene-4-sulfonic acid; trifluoroacetic acid; palladium on activated charcoal; In methanol; diethyl ether; water; N,N-dimethyl-formamide; acetonitrile; benzene;
DOI:10.1021/jm00356a004
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