1. Home
  2. 5-bromo-4-(dimethoxymethyl)pyrimidin-2-amine

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)-

5-bromo-4-(dimethoxymethyl)pyrimidin-2-amine

COC(c1nc(N)ncc1Br)OC Request for Quotation
Chemical Name: 5-bromo-4-(dimethoxymethyl)pyrimidin-2-amine
CAS Number: 914347-52-7
Product Number: AG00GV2J(AGN-PC-07A1HN)
Synonyms:
MDL No:
Molecular Formula: C7H10BrN3O2
Molecular Weight: 248.0772

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


5-Bromo-4-(dimethoxymethyl)pyrimidin-2-amine is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals due to its structural flexibility and functional group compatibility.In chemical synthesis, 5-Bromo-4-(dimethoxymethyl)pyrimidin-2-amine is commonly employed as a nucleophilic substrate for substitution reactions, enabling the introduction of diverse chemical functionalities at the bromine and amino groups. Additionally, its pyrimidine core provides a rigid and stable scaffold for the construction of more complex molecular structures, making it a valuable intermediate in the preparation of heterocyclic compounds.Furthermore, the dimethoxymethyl moiety attached to the pyrimidine ring imparts enhanced solubility and stability to the compound, facilitating its manipulation and purification during the synthesis process. This property is particularly advantageous in multistep organic reactions, where intermediate compounds need to be isolated and characterized effectively.Overall, the application of 5-Bromo-4-(dimethoxymethyl)pyrimidin-2-amine in chemical synthesis underscores its significance as a versatile and crucial component in the development of various bioactive molecules and functional materials.