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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-Cyclopentene-1-methanol

OCC1CC=CC1 Request for Quotation
Chemical Name: 3-Cyclopentene-1-methanol
CAS Number: 25125-21-7
Product Number: AG002QJP(AGN-PC-0K6A1D)
Synonyms:
MDL No: MFCD04038630
Molecular Formula: C6H10O
Molecular Weight: 98.1430

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
98.145g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
98.073g/mol
Monoisotopic Mass:
98.073g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
68.2
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Hydroxymethyl-3-cyclopentene, also known as cyclopent-3-en-1-ol, is a versatile compound used in various chemical synthesis processes. One key application of this compound lies in its potential as a building block for the synthesis of diverse chemical products. Due to its unique structure and functional groups, 1-Hydroxymethyl-3-cyclopentene can participate in reactions to form a wide range of derivatives, making it a valuable intermediate in organic synthesis.In organic chemistry, 1-Hydroxymethyl-3-cyclopentene can undergo different types of reactions such as oxidation, reduction, and substitution to yield compounds with varying chemical properties. Its presence in a molecule can influence the reactivity and stability of the entire structure, leading to the formation of complex and structurally diverse organic compounds.Furthermore, the hydroxymethyl group in 1-Hydroxymethyl-3-cyclopentene provides additional opportunities for functionalization through reactions with various reagents. This allows chemists to modify the compound further and tailor its properties for specific applications in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals.Overall, the role of 1-Hydroxymethyl-3-cyclopentene in chemical synthesis is paramount, offering chemists a valuable building block with the potential to be transformed into a wide array of compounds through strategic manipulation and utilization in various synthetic pathways.