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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)-

3-(2-Bromophenyl)pyrrolidine hydrochloride

Brc1ccccc1C1CNCC1.Cl Request for Quotation
Chemical Name: 3-(2-Bromophenyl)pyrrolidine hydrochloride
CAS Number: 1203682-28-3
Product Number: AG00HFFK(AGN-PC-0WAMII)
Synonyms:
MDL No: MFCD11223592
Molecular Formula: C10H13BrClN
Molecular Weight: 262.5739

Identification/Properties

Computed Properties
Molecular Weight:
262.575g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
260.992g/mol
Monoisotopic Mass:
260.992g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
149
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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#:
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


3-(2-Bromophenyl)pyrrolidine hydrochloride is a versatile compound widely utilized in chemical synthesis processes. This compound serves as a key building block in the creation of various advanced materials and pharmaceutical intermediates. Its unique chemical structure and reactivity make it a valuable tool for forming complex molecular structures through efficient bond formation reactions. In particular, 3-(2-Bromophenyl)pyrrolidine hydrochloride is commonly employed in the synthesis of heterocyclic compounds, which are essential components in the development of new drugs, agrochemicals, and functional materials. By incorporating this compound into synthetic pathways, chemists can access a broad range of derivatives with diverse properties and functionalities, thereby enabling the production of cutting-edge products with potential applications in medicine, agriculture, and other industries.