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

Base Information

Chemical Name:Hydrazinecarboxylic acid, 2-((5-((4-nitrophenyl)sulfonyl)-2-furanyl)iminomethyl)-, 1,1-dimethyl ester
CAS No.:75745-79-8
Molecular Formula:C₁₆H₁₈N₄O₇S
Molecular Weight:410.408
Hs Code.:
DSSTox Substance ID:DTXSID10226638

Synonyms:BRN 4595118;Hydrazinecarboxylic acid, 2-((5-((4-nitrophenyl)sulfonyl)-2-furanyl)iminomethyl)-, 1,1-dimethyl ester;75745-79-8;DTXSID10226638;LS-76681

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

Supply Marketing:

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

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

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.47g/cm³
XLogP3:2.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:6
Exact Mass:410.08962010
Heavy Atom Count:28
Complexity:713

Purity/Quality:

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)[N+](=O)[O-])N
Isomeric SMILES:CC(C)(C)OC(=O)N/N=C(/C1=CC=C(O1)S(=O)(=O)C2=CC=C(C=C2)[N+](=O)[O-])\N

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

There total 4 articles about Hydrazinecarboxylic acid, 2-((5-((4-nitrophenyl)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: 85.0%

: 870-46-2
t-butoxycarbonylhydrazine

: 349552-23-4
ethyl 5-<(4-nitrophenyl)sulphonyl>-2-furancarboximidate

: 75745-79-8
t-butylcarbonyl-5-<(4-nitrophenyl)sulphonyl>-2-furancarboxamidrazone

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

Reference yield:

: 75745-64-1
5-<(4-nitrophenyl)sulphonyl>-2-furancarbonitrile

: 75745-79-8
t-butylcarbonyl-5-<(4-nitrophenyl)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: 85 percent / methanol / 1 h / Heating

With hydrogenchloride; sodium hydrogencarbonate; In methanol;

Reference yield:

: 5-<(4-nitrophenyl)sulphonyl>-2-furancarboximidate HCl

: 75745-79-8
t-butylcarbonyl-5-<(4-nitrophenyl)sulphonyl>-2-furancarboxamidrazone

Guidance literature:: Multi-step reaction with 2 steps

1: 3percent aq. NaHCO₃ / 0.5 h / Ambient temperature

2: 85 percent / methanol / 1 h / Heating

With sodium hydrogencarbonate; In methanol;