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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)-

(6-methylpyridin-2-yl)methanamine;dihydrochloride

NCc1cccc(n1)C.Cl.Cl Request for Quotation
Chemical Name: (6-methylpyridin-2-yl)methanamine;dihydrochloride
CAS Number: 858838-82-1
Product Number: AG004R3T(AGN-PC-0IQMN8)
Synonyms:
MDL No:
Molecular Formula: C7H12Cl2N2
Molecular Weight: 195.0896

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
195.087g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
194.038g/mol
Monoisotopic Mass:
194.038g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
83
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:
3
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

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Chemical Structure


(6-Methylpyridin-2-yl)methanamine dihydrochloride, commonly referred to as $name$, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block in the development of various pharmaceuticals, agrochemicals, and advanced materials.One of the key applications of (6-Methylpyridin-2-yl)methanamine dihydrochloride is as a crucial intermediate in the synthesis of heterocyclic compounds. Its ability to undergo various functional group transformations makes it a valuable tool in the creation of complex molecular structures. Additionally, this compound can serve as a key precursor in the preparation of ligands for metal-catalyzed reactions, enabling the formation of new carbon-carbon and carbon-heteroatom bonds.Furthermore, (6-Methylpyridin-2-yl)methanamine dihydrochloride plays a vital role in the development of innovative materials such as polymers and coatings. Its unique chemical structure imparts specific properties to the final materials, enhancing their performance in various applications.Overall, the application of (6-Methylpyridin-2-yl)methanamine dihydrochloride in chemical synthesis highlights its significance in advancing the field of organic chemistry and material science, offering new possibilities for the design and preparation of novel compounds with diverse functionalities.