SZL P1-41

Base Information

Chemical Name:SZL P1-41
CAS No.:222716-34-9
Molecular Formula:C₂₄H₂₄N₂O₃S
Molecular Weight:420.532
Hs Code.:
Mol file:222716-34-9.mol

Synonyms:

Suppliers and Price of SZL P1-41

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
SZL P1-41
10mg
$ 480.00

TRC
3-(2-Benzothiazolyl)-6-ethyl-7-hydroxy-8-(1-piperidinylmethyl)-4H-1-benzopyran-4-one
50mg
$ 450.00

Tocris
SZLP1-41 ≥98%(HPLC)
10
$ 227.00

Tocris
SZLP1-41 ≥98%(HPLC)
50
$ 876.00

DC Chemicals
SZLP1-41 >98%
1 g
$ 1600.00

DC Chemicals
SZLP1-41 >98%
250 mg
$ 800.00

CSNpharm
SZLP1-41
100mg
$ 902.00

CSNpharm
SZLP1-41
1mg
$ 47.00

CSNpharm
SZLP1-41
5mg
$ 82.00

Crysdot
SZLP1-41 97%
5mg
$ 60.00

Total 11 raw suppliers

Chemical Property of SZL P1-41

Chemical Property:

Melting Point:204-207°C
Boiling Point:610.0±65.0 °C(Predicted)
PKA:6.06±0.20(Predicted)
Density:1.340±0.06 g/cm3(Predicted)
Storage Temp.:Sealed in dry,Room Temperature
Solubility.:Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)

Purity/Quality:

97% ^*data from raw suppliers

SZL P1-41 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses 3-(2-Benzothiazolyl)-6-ethyl-7-hydroxy-8-(1-piperidinylmethyl)-4H-1-benzopyran-4-one is involved in the pharmacological inactivation of Skp2 E3 ligase.

Technology Process of SZL P1-41

There total 4 articles about SZL P1-41 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: 72.0%

: 880-09-1
di(N-piperidinyl)methane

: 222716-11-2
3-(2-benzothiazolyl)-7-hydroxy-5-ethylchromone

: 222716-34-9
SZL-P1-41

Guidance literature:: In 1,4-dioxane; Heating;
DOI:10.1007/BF02311328

Reference yield:

: 2896-60-8
4-ethyl-1,3-benzenediol

: 222716-34-9
SZL-P1-41

Guidance literature:: Multi-step reaction with 3 steps

1: 67 percent / BF₃*Et₂O

2: 92 percent / piperidine / pyridine / 7 h / 120 - 130 °C

3: 72 percent / dioxane / Heating

With piperidine; boron trifluoride diethyl etherate; In 1,4-dioxane; pyridine;
DOI:10.1007/BF02311328

Reference yield:

: 56278-50-3
2-cyanomethylbenzothiazole

: 222716-34-9
SZL-P1-41

Guidance literature:: Multi-step reaction with 3 steps

1: 67 percent / BF₃*Et₂O

2: 92 percent / piperidine / pyridine / 7 h / 120 - 130 °C

3: 72 percent / dioxane / Heating

With piperidine; boron trifluoride diethyl etherate; In 1,4-dioxane; pyridine;
DOI:10.1007/BF02311328