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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)-

(1,3-dimethylpyrrolidin-3-yl)methanamine

NCC1(C)CCN(C1)C Request for Quotation
Chemical Name: (1,3-dimethylpyrrolidin-3-yl)methanamine
CAS Number: 912771-31-4
Product Number: AG00GVVP(AGN-PC-0207AC)
Synonyms:
MDL No:
Molecular Formula: C7H16N2
Molecular Weight: 128.2153

Identification/Properties

Computed Properties
Molecular Weight:
128.219g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
128.131g/mol
Monoisotopic Mass:
128.131g/mol
Topological Polar Surface Area:
29.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
103
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


1,3-Dimethyl-3-pyrrolidinemethanamine, also known as $name$, is a versatile compound widely used in chemical synthesis. One of its key applications is as a catalyst in various organic reactions. This compound plays a crucial role in promoting key transformations due to its unique structural properties.In organic synthesis, $name$ can act as a powerful base catalyst, facilitating reactions such as acylation, alkylation, and Mannich reactions. Its ability to selectively activate certain functional groups and promote specific bond-forming processes makes it a valuable tool in the production of a wide range of organic molecules.Moreover, $name$ is known for its capacity to participate in asymmetric catalysis, enabling the creation of chiral molecules with high enantiomeric purity. This feature is particularly valuable in the pharmaceutical industry, where the chirality of a molecule can significantly impact its biological activity.Overall, the application of 1,3-Dimethyl-3-pyrrolidinemethanamine in chemical synthesis serves to enhance efficiency, selectivity, and overall control in the production of complex organic compounds. Its versatility and efficacy make it a valuable asset in the toolkit of synthetic chemists seeking to design and create new molecules with precision and consistency.