Phenylalanyl-3-aminopyridine

Base Information

Chemical Name:Phenylalanyl-3-aminopyridine
CAS No.:88932-75-6
Molecular Formula:C14H15 N3 O
Molecular Weight:0
Hs Code.:
DSSTox Substance ID:DTXSID101008573
Nikkaji Number:J1.701.232K
Wikidata:Q83005071
Mol file:88932-75-6.mol

Synonyms:L-phenylalanyl-3-aminopyridine;phenylalanyl-3-aminopyridine

Suppliers and Price of Phenylalanyl-3-aminopyridine

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

Total 3 raw suppliers

Chemical Property of Phenylalanyl-3-aminopyridine

Chemical Property:

Vapor Pressure:2.15E-09mmHg at 25°C
Boiling Point:480.5°C at 760 mmHg
Flash Point:244.4°C
PSA：68.01000
Density:1.224g/cm³
LogP:2.36340
XLogP3:1.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:241.121512110
Heavy Atom Count:18
Complexity:264

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CC(C(=O)NC2=CN=CC=C2)N
Isomeric SMILES:C1=CC=C(C=C1)C[C@@H](C(=O)NC2=CN=CC=C2)N

Technology Process of Phenylalanyl-3-aminopyridine

There total 5 articles about Phenylalanyl-3-aminopyridine 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:

: 88932-69-8
3-<amino>pyridine

: 88932-75-6
3-(L-phenylalanylamino)pyridine

Guidance literature:: With hydrogenchloride; In 1,4-dioxane;
DOI:10.1021/jm030649p

Reference yield:

: 462-08-8
pyridin-3-ylamine

: 88932-75-6
3-(L-phenylalanylamino)pyridine

Guidance literature:: Multi-step reaction with 2 steps

1.1: IBCF; NMM / tetrahydrofuran

1.2: 57 percent / dimethylformamide; tetrahydrofuran / 0 - 4 °C

2.1: aq. HCl / dioxane

With 4-methyl-morpholine; hydrogenchloride; isobutyl chloroformate; In tetrahydrofuran; 1,4-dioxane;
DOI:10.1021/jm030649p

Reference yield:

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 88932-75-6
3-(L-phenylalanylamino)pyridine

Guidance literature:: Multi-step reaction with 2 steps

1.1: IBCF; NMM / tetrahydrofuran

1.2: 57 percent / dimethylformamide; tetrahydrofuran / 0 - 4 °C

2.1: aq. HCl / dioxane

With 4-methyl-morpholine; hydrogenchloride; isobutyl chloroformate; In tetrahydrofuran; 1,4-dioxane;
DOI:10.1021/jm030649p