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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)-

2-Pyrrolidinemethanamine, 1-ethyl-

NCC1CCCN1CC Request for Quotation
Chemical Name: 2-Pyrrolidinemethanamine, 1-ethyl-
CAS Number: 26116-12-1
Product Number: AG002RQK(AGN-PC-0CU1CZ)
Synonyms:
MDL No: MFCD00003178
Molecular Formula: C7H16N2
Molecular Weight: 128.2153

Identification/Properties

Properties
BP:
161.9°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.4670(lit.)
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:
29.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
83
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#:
2733
Hazard Statements:
H226-H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
3,8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Aminomethyl)-1-ethylpyrrolidine is a versatile compound widely utilized in chemical synthesis due to its unique structural properties. In organic chemistry, this compound serves as a valuable building block for the construction of various complex molecules. Its primary amine group, as well as the pyrrolidine ring, offer multiple reactive sites that can be easily functionalized through a variety of chemical reactions. This enables the synthesis of diverse organic compounds with tailored structures and properties. Additionally, the presence of the ethyl side chain provides flexibility and further possibilities for molecular modifications. Overall, 2-(Aminomethyl)-1-ethylpyrrolidine plays a crucial role in the creation of novel molecules and materials in the field of chemical synthesis.