1. Home
  2. 4-chloro-2-methylthieno[3,2-d]pyrimidine

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-chloro-2-methylthieno[3,2-d]pyrimidine

Cc1nc(Cl)c2c(n1)ccs2 Request for Quotation
Chemical Name: 4-chloro-2-methylthieno[3,2-d]pyrimidine
CAS Number: 319442-16-5
Product Number: AG0039LZ(AGN-PC-03UNDW)
Synonyms:
MDL No:
Molecular Formula: C7H5ClN2S
Molecular Weight: 184.6460

Identification/Properties

Computed Properties
Molecular Weight:
184.641g/mol
XLogP3:
2.7
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-Chloro-2-methylthieno[3,2-d]pyrimidine, or $name$, is a versatile chemical compound widely used in chemical synthesis processes. Its unique molecular structure makes it a valuable building block for the creation of various organic compounds. In chemical synthesis, this compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and materials with specialized properties.$name$ is particularly valued for its ability to participate in a variety of reactions, such as nucleophilic substitution, condensation, and cyclization reactions. Its chloro and methyl functional groups enable precise control over the reactivity and selectivity of these reactions, making it a favored choice for chemists looking to design complex molecules efficiently.Furthermore, the thieno[3,2-d]pyrimidine core of $name$ provides a stable and rigid scaffold that can be further modified to introduce additional functionalities or enhance the compound's biological activity. This flexibility makes $name$ a valuable tool in drug discovery and development, as well as in the creation of advanced materials for various industrial applications.Overall, the application of 4-Chloro-2-methylthieno[3,2-d]pyrimidine in chemical synthesis offers chemists a versatile and reliable tool for constructing diverse molecules with precision and control. Its role as a key intermediate in the synthesis of complex compounds underscores its importance in modern organic chemistry research and industry.