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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)-

1-Pyrrolidinebutanol

OCCCCN1CCCC1 Request for Quotation
Chemical Name: 1-Pyrrolidinebutanol
CAS Number: 93264-47-2
Product Number: AG00GT10(AGN-PC-00L9S4)
Synonyms:
MDL No:
Molecular Formula: C8H17NO
Molecular Weight: 143.2267

Identification/Properties

Properties
Storage:
2-8℃;Keep in dry area;
Computed Properties
Molecular Weight:
143.23g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
143.131g/mol
Monoisotopic Mass:
143.131g/mol
Topological Polar Surface Area:
23.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
79.3
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Pyrrolidin-1-yl)butan-1-ol is a versatile compound commonly used in chemical synthesis as a building block for creating a variety of complex molecules. With its unique structure combining a pyrrolidine ring and a butanol chain, this compound is valued for its ability to participate in a range of organic reactions.One key application of 4-(Pyrrolidin-1-yl)butan-1-ol is as a chiral building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its chiral nature allows for the creation of enantiomerically pure compounds, which is essential in drug discovery and development where the stereochemistry can greatly impact biological activity.In addition, this compound can serve as a nucleophile in various carbon-carbon and carbon-heteroatom bond-forming reactions. Its functional group reactivity enables the introduction of the pyrrolidine moiety into target molecules, offering a way to modify their properties and functions.Furthermore, 4-(Pyrrolidin-1-yl)butan-1-ol is utilized in the synthesis of complex natural products and materials with tailored properties. Its structural diversity and reactivity make it a valuable tool for organic chemists seeking to design and construct molecules with specific characteristics and functions.Overall, the application of 4-(Pyrrolidin-1-yl)butan-1-ol in chemical synthesis encompasses a wide range of industries and research fields, highlighting its importance as a key component in the creation of novel compounds and materials.