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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)-

2-(chloromethyl)-4,5-dihydro-1H-imidazole;hydrochloride

ClCC1=NCCN1.Cl Request for Quotation
Chemical Name: 2-(chloromethyl)-4,5-dihydro-1H-imidazole;hydrochloride
CAS Number: 13338-49-3
Product Number: AG0014R7(AGN-PC-0KKOA6)
Synonyms:
MDL No:
Molecular Formula: C4H8Cl2N2
Molecular Weight: 155.0257

Identification/Properties

Computed Properties
Molecular Weight:
155.022g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
154.006g/mol
Monoisotopic Mass:
154.006g/mol
Topological Polar Surface Area:
24.4A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
89.7
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Chloromethyl)-4,5-dihydro-1H-imidazole hydrochloride is a critical compound widely utilized in chemical synthesis processes. This versatile molecule serves as a key building block for the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure allows for the introduction of a chloromethyl group, which can participate in numerous organic reactions, such as nucleophilic substitution, addition, and condensation reactions.In chemical synthesis, 2-(Chloromethyl)-4,5-dihydro-1H-imidazole hydrochloride acts as a valuable intermediate in the production of diverse compounds due to its reactivity and compatibility with a range of functional groups. It is commonly employed as a precursor in the synthesis of biologically active compounds, including antimicrobial agents, antiviral drugs, and enzyme inhibitors. Additionally, this compound plays a crucial role in the preparation of complex organic molecules by enabling the selective modification of specific sites within a molecular framework.Overall, the strategic incorporation of 2-(Chloromethyl)-4,5-dihydro-1H-imidazole hydrochloride in chemical synthesis endeavors facilitates the efficient and streamlined production of novel chemical entities with desired properties and functionalities.