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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)-

1H-Imidazole, 4,5-dihydro-2-(phenylmethyl)-, monohydrochloride

c1ccc(cc1)CC1=NCCN1.Cl Request for Quotation
Chemical Name: 1H-Imidazole, 4,5-dihydro-2-(phenylmethyl)-, monohydrochloride
CAS Number: 59-97-2
Product Number: AG003GKZ(AGN-PC-0SU7MJ)
Synonyms:
MDL No:
Molecular Formula: C10H13ClN2
Molecular Weight: 196.6766

Identification/Properties

Properties
MP:
172-176 °C
BP:
338.2°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Stability:
Hygroscopic
Computed Properties
Molecular Weight:
196.678g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
196.077g/mol
Monoisotopic Mass:
196.077g/mol
Topological Polar Surface Area:
24.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
169
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:
2
Compound Is Canonicalized:
Yes

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

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Chemical Structure


2-Benzyl-4,5-dihydro-1H-imidazole hydrochloride, also known as $name$, serves as a versatile building block in chemical synthesis. With its unique structure, this compound plays a crucial role in various organic reactions and transformations. Due to its reactivity and stability under certain conditions, $name$ is commonly utilized in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its presence in the reaction mixture facilitates the formation of complex molecular structures and functional groups, making it an indispensable component in the synthesis of biologically active compounds. Additionally, the controlled manipulation of $name$ enables chemists to introduce specific substituents and stereochemical elements into the final products, enhancing the overall efficiency and selectivity of the synthetic process.