4-bromo-N'-butylbenzohydrazide

Base Information

Chemical Name:4-bromo-N'-butylbenzohydrazide
CAS No.:537672-41-6
Molecular Formula:C11H15BrN2O
Molecular Weight:271.15
Hs Code.:
Mol file:537672-41-6.mol

Synonyms:4-bromo-N'-butylbenzohydrazide;4-Bromobenzoic acid 2-butylhydrazide

Suppliers and Price of 4-bromo-N'-butylbenzohydrazide

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
4-Bromo-2-butylhydrazideBenzoicAcid
10mg
$ 65.00

TRC
4-Bromo-2-butylhydrazideBenzoicAcid
25mg
$ 165.00

DC Chemicals
UF010 >98%
1 g
$ 720.00

DC Chemicals
UF010 >98%
250 mg
$ 360.00

DC Chemicals
UF010 >98%
100 mg
$ 200.00

Crysdot
UF010 98+%
100mg
$ 295.00

ChemScene
UF010 99.08%
50mg
$ 180.00

ChemScene
UF010 99.08%
100mg
$ 300.00

ChemScene
UF010 99.08%
25mg
$ 100.00

ChemScene
UF010 99.08%
10mg
$ 50.00

Total 18 raw suppliers

Chemical Property of 4-bromo-N'-butylbenzohydrazide

Chemical Property:

PSA：41.13000
LogP:3.26540
Storage Temp.:Sealed in dry,Store in freezer, under -20°C
Solubility.:insoluble in H2O; ≥10.65 mg/mL in DMSO; ≥20.85 mg/mL in EtOH

Purity/Quality:

99%, ^*data from raw suppliers

4-Bromo-2-butylhydrazideBenzoicAcid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Description UF010 is a class I HDAC inhibitor with IC50 values of 0.06, 0.1, 0.5, and 1.5 μM for HDAC3, 2, 1, and 8, respectively. It is more than 6-fold selective for these class I HDACs over any additional HDACs. UF010 is reported to inhibit cancer cell proliferation with a mean GI50 value of 2.94 μM when screened against the NCI-60 panel of cancer cell lines and functions by blocking the G1/S phase of the cell cycle.

Technology Process of 4-bromo-N'-butylbenzohydrazide

There total 1 articles about 4-bromo-N'-butylbenzohydrazide 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: 58.0%

: 123-72-8
butyraldehyde

: 5933-32-4
4-bromobenzoic acid hydrazide

: 537672-41-6
4-bromo-N'-butylbenzohydrazide

Guidance literature:: butyraldehyde; 4-bromobenzoic acid hydrazide; With toluene-4-sulfonic acid; In methanol; at 20 ℃; for 12h;

With methanol; sodium cyanoborohydride; In 1,4-dioxane; at 20 ℃; for 3h;