Amidinomycin

Base Information

Chemical Name:Amidinomycin
CAS No.:3572-60-9
Molecular Formula:C₉H₁₈N₄O
Molecular Weight:198.268
Hs Code.:
UNII:A5A4FLA205
DSSTox Substance ID:DTXSID50957131
Nikkaji Number:J14.417G
Wikidata:Q27273657
Metabolomics Workbench ID:128798
ChEMBL ID:CHEMBL2392458
Mol file:3572-60-9.mol

Synonyms:amidinomycin

Suppliers and Price of Amidinomycin

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

American Custom Chemicals Corporation
AMIDINOMYCIN 95.00%
5MG
$ 501.99

Total 8 raw suppliers

Chemical Property of Amidinomycin

Chemical Property:

Refractive Index:1.6300 (estimate)
Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：104.99000
Density:1.4g/cm³
LogP:1.44730
XLogP3:-1.6
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:198.14806121
Heavy Atom Count:14
Complexity:229

Purity/Quality:

99% ^*data from raw suppliers

AMIDINOMYCIN 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CC(CC1C(=O)NCCC(=N)N)N
Isomeric SMILES:C1C[C@@H](C[C@@H]1C(=O)NCCC(=N)N)N

Technology Process of Amidinomycin

There total 8 articles about Amidinomycin 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:

: 6300-81-8,180323-33-5,180323-54-0,180323-55-1,180580-38-5
3-hydroxyimino-cyclopentanecarboxylic acid

: 3572-60-9,19946-52-2,46329-26-4,53142-01-1,150199-12-5,150199-13-6,150199-14-7
(+/-)-β--propionamidin

Guidance literature:: Multi-step reaction with 4 steps

1: H₂ / Adams catalyst / methanol

2: aq. NaOH

3: (i) SOCl₂, Py, benzene, (ii) /BRN= 1698848/, Et₂O

4: (i) HCl, EtOH, benzene, (ii) H₂, Pd-C, aq. AcOH

With sodium hydroxide; hydrogen; platinum(IV) oxide; In methanol;
DOI:10.1248/cpb.16.232

Reference yield:

: 47376-14-7,47376-16-9
(+/-)-β--propionamidin

: 3572-60-9,19946-52-2,46329-26-4,53142-01-1,150199-12-5,150199-13-6,150199-14-7
(+/-)-β--propionamidin

Guidance literature:: With hydrogen bromide; phenol; In acetic acid;
DOI:10.1002/ardp.19683010706

Reference yield:

: 19866-45-6,19866-58-1
(+/-)-β--propionitril

: 3572-60-9,19946-52-2,46329-26-4,53142-01-1,150199-12-5,150199-13-6,150199-14-7
(+/-)-β--propionamidin

Guidance literature:: Multi-step reaction with 2 steps

1: (i) EtOH, HCl, Et₂O, (ii) NH₃, EtOH

2: HBr, PhOH / acetic acid

With hydrogen bromide; phenol; In acetic acid;
DOI:10.1002/ardp.19683010706