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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)-

Piperidine, 4-[(4-methylphenyl)methyl]-

Cc1ccc(cc1)CC1CCNCC1 Request for Quotation
Chemical Name: Piperidine, 4-[(4-methylphenyl)methyl]-
CAS Number: 92822-01-0
Product Number: AG006052(AGN-PC-0KTBTJ)
Synonyms:
MDL No:
Molecular Formula: C13H19N
Molecular Weight: 189.2967

Identification/Properties

Properties
BP:
298.9°C at 760 mmHg
Storage:
2-8℃;
Computed Properties
Molecular Weight:
189.302g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
189.152g/mol
Monoisotopic Mass:
189.152g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
153
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(4-Methylbenzyl)piperidine, also known as MBP, is a versatile compound commonly utilized in chemical synthesis for its unique properties and applications. This organic compound consists of a piperidine ring with a 4-methylbenzyl group attached, making it a valuable building block in the creation of various compounds.In organic synthesis, 4-(4-Methylbenzyl)piperidine can serve as a key intermediate in the production of numerous pharmaceuticals, agrochemicals, and other specialty chemicals. Its structural features allow for effective manipulation during reactions, enabling the introduction of specific functionalities or structural modifications.Due to the presence of the piperidine ring, MBP can participate in a variety of chemical transformations such as substitutions, additions, and rearrangements, making it a valuable tool for organic chemists. This compound's versatility lends itself well to the synthesis of complex molecules, where precise control over stereochemistry and functional group compatibility is essential.Furthermore, the 4-methylbenzyl group adds steric hindrance and electron density effects, influencing the reactivity and selectivity of reactions involving 4-(4-Methylbenzyl)piperidine. This allows for fine-tuning of reaction conditions and product outcomes in chemical synthesis processes.Overall, the application of 4-(4-Methylbenzyl)piperidine in chemical synthesis provides chemists with a strategic and efficient approach to constructing diverse molecular architectures with specific properties and functionalities tailored to various industrial and research needs.