1. Home
  2. 9H-Purin-2-amine, 9-(2-bromoethyl)-6-chloro-

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)-

9H-Purin-2-amine, 9-(2-bromoethyl)-6-chloro-

BrCCn1cnc2c1nc(N)nc2Cl Request for Quotation
Chemical Name: 9H-Purin-2-amine, 9-(2-bromoethyl)-6-chloro-
CAS Number: 214201-64-6
Product Number: AG01DPLV(AGN-PC-00P1DL)
Synonyms:
MDL No:
Molecular Formula: C7H7BrClN5
Molecular Weight: 276.52098

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


9-(2-Bromoethyl)-6-chloro-9H-purin-2-amine, also known as $name$, is a versatile compound widely utilized in chemical synthesis. Its application in organic chemistry primarily lies in its ability to serve as a key building block for the synthesis of various biologically active molecules and pharmaceutical compounds. One of the notable applications of $name$ is its role as a valuable intermediate in the synthesis of nucleoside analogs. By selectively modifying the functional groups present on the purine ring, chemists can tailor the structure of nucleoside analogs to optimize desired biological activities, such as antiviral or anticancer properties. Furthermore, the reactive nature of the bromoethyl group in $name$ enables chemists to introduce additional functional groups through various chemical reactions, expanding the compound's utility in the creation of diverse molecular structures. This flexibility in chemical modification makes $name$ a valuable asset in the development of novel compounds for medicinal chemistry research and pharmaceutical applications.