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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[3,2-d]pyrimidine, 4-chloro-7-methyl-

Cc1csc2c1ncnc2Cl Request for Quotation
Chemical Name: Thieno[3,2-d]pyrimidine, 4-chloro-7-methyl-
CAS Number: 175137-21-0
Product Number: AG0020B0(AGN-PC-0KKYC3)
Synonyms:
MDL No:
Molecular Formula: C7H5ClN2S
Molecular Weight: 184.6460

Identification/Properties

Computed Properties
Molecular Weight:
184.641g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
183.986g/mol
Monoisotopic Mass:
183.986g/mol
Topological Polar Surface Area:
54A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
155
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:
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-Chloro-7-methylthieno[3,2-d]pyrimidine is a valuable building block in chemical synthesis due to its versatile reactivity and unique structural features. This compound plays a crucial role in the creation of pharmaceuticals, agrochemicals, and materials with diverse applications. In organic synthesis, 4-Chloro-7-methylthieno[3,2-d]pyrimidine can serve as a key intermediate for the synthesis of various heterocyclic compounds through functional group transformations. Its strategic placement of functional groups allows for selective reactions to occur, enabling the formation of complex molecular structures. Additionally, the presence of the thieno ring provides opportunities for further derivatization, leading to the development of novel scaffolds for drug discovery and materials science. As a result, 4-Chloro-7-methylthieno[3,2-d]pyrimidine holds significant importance in advancing synthetic methodologies and expanding the chemical space for developing innovative compounds.