1. Home
  2. 1-(6,8-difluoro-2-methylquinolin-4-yl)-3-[4-(dimethylamino)phenyl]urea

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1-(6,8-difluoro-2-methylquinolin-4-yl)-3-[4-(dimethylamino)phenyl]urea

O=C(Nc1cc(C)nc2c1cc(F)cc2F)Nc1ccc(cc1)N(C)C Request for Quotation
Chemical Name: 1-(6,8-difluoro-2-methylquinolin-4-yl)-3-[4-(dimethylamino)phenyl]urea
CAS Number: 288150-92-5
Product Number: AG002WLQ(AGN-PC-0L9BFI)
Synonyms:
MDL No:
Molecular Formula: C19H18F2N4O
Molecular Weight: 356.3692

Identification/Properties

Properties
BP:
430.3±45.0 °C(Predicted)
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Solubility:
DMSO: ~24 mg/mL
Computed Properties
Molecular Weight:
356.377g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
356.145g/mol
Monoisotopic Mass:
356.145g/mol
Topological Polar Surface Area:
57.3A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
484
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Derived from meticulous scientific research, SB-408124 has emerged as a pivotal agent in the realm of chemical synthesis. With its exceptional properties, this versatile compound serves as a catalyst of transformation in the field of organic chemistry. By facilitating intricate reactions and promoting molecular rearrangements, SB-408124 enables targeted modifications with unparalleled precision. Its strategic utility in initiating key steps of synthesis procedures underscores its indispensable role in advancing the frontiers of chemical innovation.