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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-Pyrrolidinemethanamine, N,N-dimethyl-

CN(CC1CNCC1)C Request for Quotation
Chemical Name: 3-Pyrrolidinemethanamine, N,N-dimethyl-
CAS Number: 99724-17-1
Product Number: AG0064SR(AGN-PC-000CQV)
Synonyms:
MDL No:
Molecular Formula: C7H16N2
Molecular Weight: 128.2153

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
128.219g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
128.131g/mol
Monoisotopic Mass:
128.131g/mol
Topological Polar Surface Area:
15.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
81
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:
Danger
UN#:
2735
Hazard Statements:
H302-H314-H332
Precautionary Statements:
P260-P261-P264-P270-P271-P280-P301+P312-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P312-P321-P330-P363-P405-P501
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


N,N-Dimethyl-1-(pyrrolidin-3-yl)methanamine serves as a valuable reagent in chemical synthesis, specifically in the realm of organic chemistry. This compound, with its unique structure incorporating a pyrrolidine ring, finds wide application as a versatile building block for the synthesis of various pharmaceuticals, agrochemicals, and materials. Its presence in a molecule can confer enhanced biological activities or alter the physicochemical properties of the resulting product. With its ability to participate in a range of chemical reactions, N,N-Dimethyl-1-(pyrrolidin-3-yl)methanamine plays a crucial role in the creation of intricate molecular architectures, making it a key component in the toolkit of synthetic chemists seeking to design novel compounds with tailored functionalities.