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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-phenylpyrrolidin-3-yl)methanol

OCC1CCN(C1)c1ccccc1 Request for Quotation
Chemical Name: (1-phenylpyrrolidin-3-yl)methanol
CAS Number: 99858-80-7
Product Number: AG004X7A(AGN-PC-01NOYC)
Synonyms:
MDL No: MFCD08059754
Molecular Formula: C11H15NO
Molecular Weight: 177.2429

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
177.247g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
177.115g/mol
Monoisotopic Mass:
177.115g/mol
Topological Polar Surface Area:
23.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
154
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(1-Phenylpyrrolidin-3-yl)methanol, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and properties make it a valuable compound in the development of various organic molecules.One of the key applications of (1-Phenylpyrrolidin-3-yl)methanol is its use as a chiral auxiliary in asymmetric synthesis. This compound can serve as a scaffold for creating enantiomerically pure products, which is essential in the pharmaceutical and agrochemical industries where the stereochemistry of the molecules greatly influences their biological activity.Moreover, (1-Phenylpyrrolidin-3-yl)methanol can be utilized in the synthesis of complex natural products and drug candidates. By incorporating this compound into the chemical reaction pathway, chemists can control the stereochemistry and overall efficiency of the synthesis process, leading to the production of valuable compounds with high purity and yield.Additionally, (1-Phenylpyrrolidin-3-yl)methanol can be employed in the preparation of ligands for catalytic reactions or in the construction of molecular frameworks with specific functionalities. Its ability to participate in diverse chemical transformations makes it a valuable tool for organic chemists seeking to access a wide range of structurally diverse compounds for various applications.Overall, the versatile nature of (1-Phenylpyrrolidin-3-yl)methanol makes it an indispensable component in the toolbox of synthetic chemists, enabling innovative strategies for the synthesis of complex molecules with precise control over stereochemistry and functionality.