1. Home
  2. 2-Chloro-5-iodo-7H-pyrrolo[2,3-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)-

2-Chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine

Clc1ncc2c(n1)[nH]cc2I Request for Quotation
Chemical Name: 2-Chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine
CAS Number: 1060815-90-8
Product Number: AG0084EN(AGN-PC-09LIUC)
Synonyms:
MDL No:
Molecular Formula: C6H3ClIN3
Molecular Weight: 279.4656

Identification/Properties

Computed Properties
Molecular Weight:
279.465g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
278.906g/mol
Monoisotopic Mass:
278.906g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
157
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


2-Chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine is a versatile intermediate compound widely utilized in chemical synthesis. Due to its unique molecular structure, this compound serves as a valuable building block in the creation of complex organic molecules. Its strategic placement of chloro and iodo groups enables selective functionalization and facilitates diverse chemical transformations.In the realm of chemical synthesis, 2-Chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine is frequently employed as a key starting material for the synthesis of biologically active compounds, pharmaceuticals, and agrochemicals. Its structural features make it a valuable precursor for the introduction of specific functional groups, enabling the generation of novel molecules with enhanced properties and bioactivities.Moreover, the reactivity of 2-Chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine allows for the construction of intricate molecular frameworks through coupling reactions, cascade reactions, and other synthetic methodologies. Its structural complexity and compatibility with various synthetic strategies make it a versatile and indispensable component in the toolbox of organic chemists and researchers working in drug discovery, materials science, and other related fields.Overall, the strategic incorporation of 2-Chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine in chemical synthesis enables efficient access to diverse molecular architectures with potential applications in medicinal chemistry, materials design, and beyond.