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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)-

4-(7-chlorophthalazin-1-yl)morpholine

Clc1ccc2c(c1)c(nnc2)N1CCOCC1 Request for Quotation
Chemical Name: 4-(7-chlorophthalazin-1-yl)morpholine
CAS Number: 951885-55-5
Product Number: AG003K5O(AGN-PC-0570FV)
Synonyms:
MDL No:
Molecular Formula: C12H12ClN3O
Molecular Weight: 249.6962

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
249.698g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
249.067g/mol
Monoisotopic Mass:
249.067g/mol
Topological Polar Surface Area:
38.2A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
260
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 4-(7-Chlorophthalazin-1-yl)morpholine compound serves as a versatile building block in chemical synthesis processes. Offering a unique combination of a phthalazine ring and a morpholine group, this compound finds wide application in pharmaceutical and agrochemical industries as a key intermediate for the synthesis of various biologically active compounds. Its structural features make it particularly valuable for the development of novel drugs and crop protection agents. The presence of the chloro group provides opportunities for further functionalization, allowing for the creation of diverse derivatives with enhanced properties. In organic synthesis, this compound can be utilized to introduce the phthalazine-morpholine motif into complex molecular structures, enabling the design of molecules with specific biological activities or chemical reactivity. Its use in the construction of heterocyclic frameworks highlights its significance as a valuable tool for expanding the chemical space and exploring new applications in the field of medicinal and agricultural chemistry.