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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)-

Benzenemethanamine, 2-chloro-N-methyl-

CNCc1ccccc1Cl Request for Quotation
Chemical Name: Benzenemethanamine, 2-chloro-N-methyl-
CAS Number: 94-64-4
Product Number: AG005VYZ(AGN-PC-0JL7DF)
Synonyms:
MDL No:
Molecular Formula: C8H10ClN
Molecular Weight: 155.6247

Identification/Properties

Properties
MP:
0 °C
BP:
206.9°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
155.625g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
155.05g/mol
Monoisotopic Mass:
155.05g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
95.3
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:
Danger
UN#:
2735
Hazard Statements:
H302-H315-H318-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-N-methylbenzylamine is a versatile compound widely used in chemical synthesis for various applications. Its primary role lies in the field of organic chemistry, specifically in the development of pharmaceuticals and agrochemicals. The unique structure of 2-Chloro-N-methylbenzylamine makes it a valuable building block for the synthesis of complex molecules and active pharmaceutical ingredients.One of the key applications of 2-Chloro-N-methylbenzylamine is in the synthesis of heterocyclic compounds, which are crucial components in the development of numerous medicinal drugs. By serving as a starting material or intermediate in the synthesis process, this compound facilitates the creation of diverse chemical structures with specific biological activities.Furthermore, 2-Chloro-N-methylbenzylamine's reactivity and functional groups enable the formation of various derivatives through chemical transformations. These derivatives can have modified properties, enhancing their effectiveness in specific applications or improving their compatibility with target molecules.In summary, 2-Chloro-N-methylbenzylamine plays a significant role in chemical synthesis by serving as a key component in the construction of complex molecules, particularly in the pharmaceutical and agrochemical industries. Its versatility and reactivity make it a valuable tool for scientists and researchers striving to develop innovative compounds with potential therapeutic or agricultural benefits.