N~2~-isopropyl-2,5-pyridinediamine

Base Information

Chemical Name:N~2~-isopropyl-2,5-pyridinediamine
CAS No.:52025-41-9
Molecular Formula:C₈H₁₃N₃
Molecular Weight:151.211
Hs Code.:
DSSTox Substance ID:DTXSID701281707
Mol file:52025-41-9.mol

Synonyms:52025-41-9;N~2~-isopropyl-2,5-pyridinediamine;n2-isopropylpyridine-2,5-diamine;N2-Isopropyl-2,5-pyridinediamine;2-N-propan-2-ylpyridine-2,5-diamine;SCHEMBL13249613;GIFWHQBUBNUEBY-UHFFFAOYSA-N;DTXSID701281707;MFCD09047761;AKOS000131411;N*2*-isopropyl-pyridine-2,5-diamine;MCULE-3020781709;N2-(propan-2-yl)pyridine-2,5-diamine;DA-42217;N2-(1-Methylethyl)-2,5-pyridinediamine;CS-0227233;EN300-58665;N~2~-isopropyl-2,5-pyridinediamine(SALTDATA: FREE)

Suppliers and Price of N~2~-isopropyl-2,5-pyridinediamine

Supply Marketing:

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

TRC
N2-isopropyl-2,5-pyridinediamine
50mg
$ 155.00

TRC
N2-isopropyl-2,5-pyridinediamine
10mg
$ 45.00

Matrix Scientific
N2-Isopropyl-2,5-pyridinediamine
1g
$ 432.00

Matrix Scientific
N2-Isopropyl-2,5-pyridinediamine
10g
$ 1602.00

Matrix Scientific
N2-Isopropyl-2,5-pyridinediamine
5g
$ 1206.00

American Custom Chemicals Corporation
2-N-(PROPAN-2-YL)PYRIDINE-2,5-DIAMINE 95.00%
1G
$ 764.03

Total 6 raw suppliers

Chemical Property of N~2~-isopropyl-2,5-pyridinediamine

Chemical Property:

XLogP3:1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:151.110947427
Heavy Atom Count:11
Complexity:114

Purity/Quality:

97% ^*data from raw suppliers

N2-isopropyl-2,5-pyridinediamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)NC1=NC=C(C=C1)N

Technology Process of N~2~-isopropyl-2,5-pyridinediamine

There total 1 articles about N~2~-isopropyl-2,5-pyridinediamine 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:

: 4487-59-6
2-bromo-5-nitropyridine

: 52025-41-9
N²-isopropylpyridine-2,5-diamine

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In methanol; at 20 ℃; for 18h;

Reference yield:

: 52025-41-9
N²-isopropylpyridine-2,5-diamine

: 1103234-38-3
6-chloro-2-fluoro-3-(propane-1-sulfonylamino)benzoyl chloride

: 1103232-13-8
6-chloro-2-fluoro-N-(6-isopropylaminopyridin-3-yl)-3-(propane-1-sulfonylamino)benzamide

Guidance literature:: With triethylamine; In tetrahydrofuran; at 20 ℃; for 20h; Cooling with ice/salt bath;

Reference yield:

: 52025-41-9
N²-isopropylpyridine-2,5-diamine

: 4-(1-(6-(isopropylamino)pyridin-3-yl)-1H-1,2,3-triazol-4-yl)benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogenchloride; sodium nitrite / ethyl acetate; water / 0.5 h / 0 °C

1.2: 2 h / 0 - 20 °C

2.1: sodium L-ascorbate; copper(II) sulfate heptahydrate; N-ethyl-N,N-diisopropylamine / water; methanol / 16 h / 20 °C / Inert atmosphere

With hydrogenchloride; copper(II) sulfate heptahydrate; sodium L-ascorbate; N-ethyl-N,N-diisopropylamine; sodium nitrite; In methanol; water; ethyl acetate;
DOI:10.1016/j.ejmech.2020.112525