1-METHYL-BIO

Base Information

Chemical Name:1-METHYL-BIO
CAS No.:667463-95-8
Molecular Formula:C17H12BrN3O2
Molecular Weight:370.20000
Hs Code.:
Mol file:667463-95-8.mol

Synonyms:IN1310;methyl-6BIO;6-bromo-1-methylindirubin-3'-oxime;

Suppliers and Price of 1-METHYL-BIO

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

Usbiological
MeBIO
10mg
$ 418.00

Usbiological
MeBIO
1mg
$ 368.00

TRC
MeBIO
1mg
$ 95.00

Tocris
MeBIO ≥99%(HPLC)
10
$ 169.00

Cayman Chemical
MeBIO ≥95%
5mg
$ 89.00

Cayman Chemical
MeBIO ≥95%
10mg
$ 150.00

Cayman Chemical
MeBIO ≥95%
1mg
$ 28.00

ApexBio Technology
MeBIO
10mg
$ 192.00

American Custom Chemicals Corporation
GSK-3 INHIBITOR (XIV) 95.00%
1MG
$ 658.53

AK Scientific
MeBIO
10mg
$ 286.00

Total 9 raw suppliers

Chemical Property of 1-METHYL-BIO

Chemical Property:

PSA：64.93000
LogP:1.44850
Storage Temp.:Store at +4°C

Purity/Quality:

97% ^*data from raw suppliers

MeBIO ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses MeBIO is an indirubin, which has been suggested to possess the structural basis for a potent and selective inhibitor of glycogen synthase kinase-3 (GSK3) and cyclin-dependent kinases.

Technology Process of 1-METHYL-BIO

There total 7 articles about 1-METHYL-BIO 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:

: 667463-98-1
1-Methyl-6-bromoindirubin

: 667463-95-8,710323-61-8
MeBIO

Guidance literature:: With pyridine; hydroxylamine hydrochloride; at 120 ℃; for 1.5h;
DOI:10.1021/jm031016d

Reference yield:

: 6326-79-0
6-bromoisatin

: 667463-95-8,710323-61-8
MeBIO

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / Na₂CO₃ / acetone / 2 h / 60 °C

2: 49 percent / Na₂CO₃ / methanol / 3 h

3: pyridine; H₂NOH*HCl / 1.5 h / 120 °C

With pyridine; hydroxylamine hydrochloride; sodium carbonate; In methanol; acetone;
DOI:10.1021/jm031016d

Reference yield:

: 667463-64-1
6-bromo-N-methylisatin

: 667463-95-8,710323-61-8
MeBIO

Guidance literature:: Multi-step reaction with 2 steps

1: 49 percent / Na₂CO₃ / methanol / 3 h

2: pyridine; H₂NOH*HCl / 1.5 h / 120 °C

With pyridine; hydroxylamine hydrochloride; sodium carbonate; In methanol;
DOI:10.1021/jm031016d