(3S)-1-(4-Nitrophenyl)-3-pyrrolidinamine

Base Information

Chemical Name:(3S)-1-(4-Nitrophenyl)-3-pyrrolidinamine
CAS No.:202267-29-6
Molecular Formula:C₁₀H₁₃N₃O₂
Molecular Weight:207.232
Hs Code.:
DSSTox Substance ID:DTXSID501274659

Synonyms:(3S)-1-(4-Nitrophenyl)-3-pyrrolidinamine;SCHEMBL6873751;DTXSID501274659;202267-29-6

Suppliers and Price of (3S)-1-(4-Nitrophenyl)-3-pyrrolidinamine

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of (3S)-1-(4-Nitrophenyl)-3-pyrrolidinamine

Chemical Property:

XLogP3:1.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:207.100776666
Heavy Atom Count:15
Complexity:233

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CN(CC1N)C2=CC=C(C=C2)[N+](=O)[O-]
Isomeric SMILES:C1CN(C[C@H]1N)C2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of (3S)-1-(4-Nitrophenyl)-3-pyrrolidinamine

There total 4 articles about (3S)-1-(4-Nitrophenyl)-3-pyrrolidinamine 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:

: 202267-28-5
1-(4-nitro)phenyl-3(S)-trifluoroacetylaminopyrrolidine

: 202267-29-6
3(S)-amino-1-(4-nitro)phenylpyrrolidine

Guidance literature:: With potassium carbonate; In methanol; water;

Reference yield:

: 862686-31-5
tert-butyl [(3S)-(4-nitrophenyl)pyrrolidin-3-yl]carbamate

: 202267-29-6
3(S)-amino-1-(4-nitro)phenylpyrrolidine

Guidance literature:: With hydrogenchloride; acetic acid; In water; at 20 ℃; for 2h;
DOI:10.1021/jm2000773

Reference yield:

: 350-46-9,178603-76-4
4-Fluoronitrobenzene

: 202267-29-6
3(S)-amino-1-(4-nitro)phenylpyrrolidine

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile / 48 h / Reflux

2: hydrogenchloride; acetic acid / water / 2 h / 20 °C

With hydrogenchloride; potassium carbonate; acetic acid; In water; acetonitrile;
DOI:10.1021/jm2000773