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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)-

(trans-4-methylpyrrolidin-3-yl)methanol

C[C@H]1CNC[C@@H]1CO Request for Quotation
Chemical Name: (trans-4-methylpyrrolidin-3-yl)methanol
CAS Number: 945723-36-4
Product Number: AG00IICK(AGN-PC-0ONWY6)
Synonyms:
MDL No:
Molecular Formula: C6H13NO
Molecular Weight: 115.1735

Identification/Properties

Computed Properties
Molecular Weight:
115.176g/mol
XLogP3:
-0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
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:
74.9
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:
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


The (trans-4-Methylpyrrolidin-3-yl)methanol, commonly known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Due to its unique structure, $name$ demonstrates excellent reactivity and selectivity when utilized in organic reactions. In the realm of chemical synthesis, this compound serves as a valuable intermediate for the production of various pharmaceuticals, agrochemicals, and specialty chemicals.As a key component in the synthesis of complex organic molecules, $name$ facilitates the formation of diverse chemical bonds through its functional groups. Its ability to undergo selective transformations makes it a preferred choice for the construction of intricate molecular structures. Chemists leverage the synthetic potential of $name$ in the creation of innovative drug candidates, fine chemicals, and advanced materials.Furthermore, the presence of the pyrrolidine ring in the molecular framework of $name$ imparts additional versatility to its synthetic applications. This cyclic structure confers chirality and stereochemical control in chemical transformations, enabling the synthesis of enantiomerically pure compounds. By harnessing the reactivity of $name$, chemists can access a wide array of stereochemically complex molecules with high precision and efficiency.In summary, the application of (trans-4-Methylpyrrolidin-3-yl)methanol in chemical synthesis encompasses its pivotal role as a valuable building block for the efficient construction of complex organic molecules. Leveraging its reactivity, selectivity, and stereochemical influence, chemists can drive innovation in drug discovery, materials science, and various other fields of organic chemistry.