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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, 4-chloro-

Clc1ncnc2c1ccs2 Request for Quotation
Chemical Name: Thieno[2,3-d]pyrimidine, 4-chloro-
CAS Number: 14080-59-2
Product Number: AG001CSN(AGN-PC-0C5OOC)
Synonyms:
MDL No:
Molecular Formula: C6H3ClN2S
Molecular Weight: 170.6194

Identification/Properties

Computed Properties
Molecular Weight:
170.614g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
169.971g/mol
Monoisotopic Mass:
169.971g/mol
Topological Polar Surface Area:
54A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
133
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

NMR Spectrum

PNMR/4-Chlorothieno23-dpyrimidine-14080-59-2-hnmr.pdf

Other Analytical Data

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Chemical Structure


4-Chlorothieno[2,3-d]pyrimidine is a versatile heterocyclic compound that finds widespread application in chemical synthesis. As a key building block in organic chemistry, this compound serves as a crucial intermediate in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Due to its unique structure and reactivity, 4-Chlorothieno[2,3-d]pyrimidine is commonly employed in the synthesis of complex molecules with biological activity. Its incorporation into organic frameworks enables the creation of diverse chemical entities with valuable properties, making it a valuable tool for synthetic chemists seeking to develop new compounds with therapeutic or commercial potential.