Thieno[2,3-d]pyrimidine, 4-chloro-|14080-59-2,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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-

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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
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NMR Spectrum
Other Analytical Data
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Identification/Properties

Computed Properties

Molecular Weight:

170.614g/mol

XLogP3:

2.1

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

169.971g/mol

Monoisotopic Mass:

169.971g/mol

Topological Polar Surface Area:

54A^2

Heavy Atom Count:

Formal Charge:

Complexity:

133

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

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.