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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-Pyrrolidineethanol

OCCC1CNCC1 Request for Quotation
Chemical Name: 3-Pyrrolidineethanol
CAS Number: 931-44-2
Product Number: AG006IAW(AGN-PC-04QKGG)
Synonyms:
MDL No:
Molecular Formula: C6H13NO
Molecular Weight: 115.1735

Identification/Properties

Properties
BP:
201.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
115.176g/mol
XLogP3:
-0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
115.1g/mol
Monoisotopic Mass:
115.1g/mol
Topological Polar Surface Area:
32.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
65.5
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
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


2-(Pyrrolidin-3-yl)ethanol, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound serves as a key building block for the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. When used in chemical synthesis, 2-(Pyrrolidin-3-yl)ethanol acts as a valuable intermediate in the production of functionalized heterocycles and complex organic molecules. Its unique structure enables efficient incorporation into synthetic pathways, allowing for the modification and enhancement of desired chemical properties. Additionally, the presence of the pyrrolidine ring confers specific stereochemical characteristics that are crucial for the development of chiral molecules with potential biological activity. In summary, the application of 2-(Pyrrolidin-3-yl)ethanol in chemical synthesis facilitates the creation of diverse compounds with tailored structures and functionalities.