1. Home
  2. 4-(dimethoxymethyl)pyridin-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)-

4-(dimethoxymethyl)pyridin-2-amine

COC(c1ccnc(c1)N)OC Request for Quotation
Chemical Name: 4-(dimethoxymethyl)pyridin-2-amine
CAS Number: 889945-19-1
Product Number: AG00451D(AGN-PC-09S2ST)
Synonyms:
MDL No:
Molecular Formula: C8H12N2O2
Molecular Weight: 168.1931

Identification/Properties

Properties
BP:
268.3°C at 760 mmHg
Storage:
2-8℃;
Computed Properties
Molecular Weight:
168.196g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
168.09g/mol
Monoisotopic Mass:
168.09g/mol
Topological Polar Surface Area:
57.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
128
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

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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-(Dimethoxymethyl)pyridin-2-amine is a highly versatile compound that finds significant application in chemical synthesis processes. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and other organic products. Specifically, 4-(Dimethoxymethyl)pyridin-2-amine is frequently used as a key intermediate in the synthesis of biologically active molecules and functionalized heterocycles. Its unique structure offers a range of opportunities for derivatization, enabling chemists to modify and manipulate its reactivity to achieve diverse chemical transformations. The presence of the pyridine ring confers distinct properties to the compound, making it a valuable tool in the design and development of new chemical entities with potential applications in the fields of medicine, agriculture, and materials science. Through strategic incorporation of 4-(Dimethoxymethyl)pyridin-2-amine into synthetic pathways, chemists can access novel compounds with enhanced biological activity, improved selectivity, and desirable physicochemical properties. Its role as a synthetic building block underscores its importance in modern chemical synthesis strategies, contributing to the advancement of drug discovery, agrochemical development, and innovative material design.