Mitomycin K

Base Information

Chemical Name:Mitomycin K
CAS No.:74148-45-1
Molecular Formula:C16H18N2O4
Molecular Weight:302.33
Hs Code.:
DSSTox Substance ID:DTXSID40995587
Nikkaji Number:J551.550E
ChEMBL ID:CHEMBL284124

Synonyms:Mitomycin K;74148-45-1;Azirino(2',3':3,4)pyrrolo(1,2-a)indole-4,7-dione, 1,1a,2,8,8a,8b-hexahydro-6,8a-dimethoxy-1,5-dimethyl-8-methylene-, (1aS-(1a-alpha,8a-alpha,8b-alpha))-;CHEMBL284124;DTXSID40995587;LS-23422;6,8a-Dimethoxy-1,5-dimethyl-8-methylidene-1,1a,2,8,8a,8b-hexahydroazireno[2',3':3,4]pyrrolo[1,2-a]indole-4,7-dione

Suppliers and Price of Mitomycin K

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
MITOMYCIN K 95.00%
5MG
$ 504.28

Total 0 raw suppliers

Chemical Property of Mitomycin K

Chemical Property:

Melting Point:92-93 °C
Boiling Point:463.7°Cat760mmHg
Flash Point:234.3°C
PSA：58.85000
Density:1.37g/cm³
LogP:0.09920
XLogP3:0.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:2
Exact Mass:302.12665706
Heavy Atom Count:22
Complexity:720

Purity/Quality:: MITOMYCIN K 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C(=O)C2=C(C1=O)N3CC4C(C3(C2=C)OC)N4C)OC
Isomeric SMILES:CC1=C(C(=O)C2=C(C1=O)N3C[C@H]4[C@@H]([C@@]3(C2=C)OC)N4C)OC

Technology Process of Mitomycin K

There total 1 articles about Mitomycin K 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:

: 4055-40-7
mitomycin B

: 74148-45-1
(+)-mitomycin K

Guidance literature:: Multi-step reaction with 2 steps

1: 60 percent / 1,8-diazabicyclo<5.4.0>undec-7-ene / tetrahydrofuran / 120 h / 5 °C

2: 79 percent / sodium hydride / benzene; dimethylformamide / 0.33 h / -15 °C

With sodium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; N,N-dimethyl-formamide; benzene;