Hydrazinecarboxylic acid, 2-((5-((4-methoxyphenyl)sulfonyl)-2-furanyl)iminomethyl)-, 1,1-dimethyl ester

Base Information

Chemical Name:Hydrazinecarboxylic acid, 2-((5-((4-methoxyphenyl)sulfonyl)-2-furanyl)iminomethyl)-, 1,1-dimethyl ester
CAS No.:75745-78-7
Molecular Formula:C₁₇H₂₁N₃O₆S
Molecular Weight:395.436
Hs Code.:
DSSTox Substance ID:DTXSID50226637
Mol file:75745-78-7.mol

Synonyms:BRN 4580153;75745-78-7;Hydrazinecarboxylic acid, 2-((5-((4-methoxyphenyl)sulfonyl)-2-furanyl)iminomethyl)-, 1,1-dimethyl ester;C17H21N3O6S;C17-H21-N3-O6-S;DTXSID50226637;LS-76679

Suppliers and Price of Hydrazinecarboxylic acid, 2-((5-((4-methoxyphenyl)sulfonyl)-2-furanyl)iminomethyl)-, 1,1-dimethyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 1 raw suppliers

Chemical Property of Hydrazinecarboxylic acid, 2-((5-((4-methoxyphenyl)sulfonyl)-2-furanyl)iminomethyl)-, 1,1-dimethyl ester

Chemical Property:

Density:1.344g/cm³
XLogP3:2.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:7
Exact Mass:395.11510657
Heavy Atom Count:27
Complexity:645

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NN=C(C1=CC=C(O1)S(=O)(=O)C2=CC=C(C=C2)OC)N
Isomeric SMILES:CC(C)(C)OC(=O)N/N=C(/C1=CC=C(O1)S(=O)(=O)C2=CC=C(C=C2)OC)\N

Technology Process of Hydrazinecarboxylic acid, 2-((5-((4-methoxyphenyl)sulfonyl)-2-furanyl)iminomethyl)-, 1,1-dimethyl ester

There total 4 articles about Hydrazinecarboxylic acid, 2-((5-((4-methoxyphenyl)sulfonyl)-2-furanyl)iminomethyl)-, 1,1-dimethyl 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:

Reference yield: 80.0%

: 870-46-2
t-butoxycarbonylhydrazine

: 349551-52-6
ethyl 5-<(4-methoxyphenyl)sulphonyl>-2-furancarboximidate

: 75745-78-7
t-butoxycarbonyl-5-<(4-methoxyphenyl)sulphonyl>-2-furancarboxamidrazone

Guidance literature:: In methanol; for 1h; Heating;

Reference yield:

: 61942-33-4
5-<(4-methoxyphenyl)sulphonyl>-2-furancarboxaldehyde

: 75745-78-7
t-butoxycarbonyl-5-<(4-methoxyphenyl)sulphonyl>-2-furancarboxamidrazone

Guidance literature:: Multi-step reaction with 4 steps

1: 80 percent / NH₂OH*HCl, Ac₂O / methanol / 1 h / Heating

2: HCl(g) / 48 h / 0 - 5 °C

3: 3percent aq. NaHCO₃ / 0.5 h / Ambient temperature

4: 80 percent / methanol / 1 h / Heating

With hydrogenchloride; hydroxylamine hydrochloride; acetic anhydride; sodium hydrogencarbonate; In methanol;

Reference yield:

: 75745-63-0
5-<(4-methoxyphenyl)sulphonyl>-2-furancarbonitrile

: 75745-78-7
t-butoxycarbonyl-5-<(4-methoxyphenyl)sulphonyl>-2-furancarboxamidrazone

Guidance literature:: Multi-step reaction with 3 steps

1: HCl(g) / 48 h / 0 - 5 °C

2: 3percent aq. NaHCO₃ / 0.5 h / Ambient temperature

3: 80 percent / methanol / 1 h / Heating

With hydrogenchloride; sodium hydrogencarbonate; In methanol;