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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-Cyclopentene-1-methanol, 4-amino-, hydrochloride, (1S,4R)-

N[C@@H]1C[C@@H](C=C1)CO.Cl Request for Quotation
Chemical Name: 2-Cyclopentene-1-methanol, 4-amino-, hydrochloride, (1S,4R)-
CAS Number: 168960-19-8
Product Number: AG001YF8(AGN-PC-0O4S3J)
Synonyms:
MDL No:
Molecular Formula: C6H12ClNO
Molecular Weight: 149.6186

Identification/Properties

Computed Properties
Molecular Weight:
149.618g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
149.061g/mol
Monoisotopic Mass:
149.061g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
101
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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#:
N/A
Hazard Statements:
H317-H412
Precautionary Statements:
P273-P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The chiral compound ((1S,4R)-4-Aminocyclopent-2-en-1-yl)methanol hydrochloride holds significant utility in chemical synthesis as a versatile building block. With its unique structural arrangement and stereochemistry, this compound serves as a valuable precursor in the creation of various complex molecules. The presence of both an amino group and a hydroxyl group provides multiple reactive sites for derivatization and functionalization, allowing for tailored modifications in synthetic pathways. Additionally, the cyclopentene ring confers rigidity and spatial orientation to the molecule, enabling specific molecular arrangements in target compounds. Through strategic utilization of ((1S,4R)-4-Aminocyclopent-2-en-1-yl)methanol hydrochloride in chemical transformations, researchers can access structurally diverse compounds with enhanced stereochemical control and potential biological activity.