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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)-

Thieno[2,3-d]pyrimidine, 2-chloro-4-(4-morpholinyl)-

Clc1nc(N2CCOCC2)c2c(n1)scc2 Request for Quotation
Chemical Name: Thieno[2,3-d]pyrimidine, 2-chloro-4-(4-morpholinyl)-
CAS Number: 63894-67-7
Product Number: AG00EIJ1(AGN-PC-00KKNL)
Synonyms:
MDL No:
Molecular Formula: C10H10ClN3OS
Molecular Weight: 255.7239

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
255.72g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
255.023g/mol
Monoisotopic Mass:
255.023g/mol
Topological Polar Surface Area:
66.5A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
252
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(2-Chlorothieno[2,3-d]pyrimidin-4-yl)morpholine is a versatile compound that finds application in chemical synthesis as a key building block in the creation of pharmaceuticals, agrochemicals, and materials science. With its unique structure combining a chlorothieno-pyrimidine core with a morpholine moiety, this compound serves as a valuable intermediate in the development of novel organic molecules.In chemical synthesis, 4-(2-Chlorothieno[2,3-d]pyrimidin-4-yl)morpholine acts as a crucial component for the construction of biologically active compounds, such as potential drug candidates or pesticides. Its specific molecular structure allows for the introduction of diverse functional groups, enabling the modification of its chemical properties to achieve desired pharmacological or agricultural effects.Furthermore, the incorporation of 4-(2-Chlorothieno[2,3-d]pyrimidin-4-yl)morpholine into synthetic pathways offers synthetic chemists a strategic tool for accessing complex molecular frameworks efficiently. Its compatibility with various reaction conditions and its ability to selectively participate in key transformations make it a valuable asset in the synthesis of target compounds with tailored properties.Overall, the utility of 4-(2-Chlorothieno[2,3-d]pyrimidin-4-yl)morpholine in chemical synthesis highlights its significance as a versatile building block with diverse applications in the creation of functional molecules across different fields of chemistry.