1. Home
  2. 3-(methoxymethyl)pyrrolidine

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-(methoxymethyl)pyrrolidine

COCC1CNCC1 Request for Quotation
Chemical Name: 3-(methoxymethyl)pyrrolidine
CAS Number: 936940-38-4
Product Number: AG0036SW(AGN-PC-03XTXJ)
Synonyms:
MDL No:
Molecular Formula: C6H13NO
Molecular Weight: 115.1735

Identification/Properties

Properties
BP:
141.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
115.176g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
115.1g/mol
Monoisotopic Mass:
115.1g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
65.5
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
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#:
1993
Hazard Statements:
H226-H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
3
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


3-(Methoxymethyl)pyrrolidine is a valuable compound commonly utilized in chemical synthesis as a versatile building block. Its unique structure contains a pyrrolidine ring with a methoxymethyl functional group attached at the third position, offering a range of synthetic opportunities in various organic transformations.Firstly, 3-(Methoxymethyl)pyrrolidine is frequently employed as a protecting group for amines in organic synthesis. By selectively masking the amino functionality with the methoxymethyl group, chemists can prevent unwanted reactions or side reactions during the synthesis of complex molecules. This protective strategy enables the targeted modification of specific functional groups while maintaining the overall integrity of the molecule.Secondly, the presence of the methoxymethyl moiety in 3-(Methoxymethyl)pyrrolidine offers a handle for further derivatization. The ether linkage can be easily manipulated through cleavage or substitution reactions, allowing for the introduction of additional functionalities or structural modifications. This flexibility is particularly advantageous in the construction of pharmaceutical intermediates or natural product analogs, where precise control over the molecular architecture is essential.Lastly, 3-(Methoxymethyl)pyrrolidine serves as a valuable precursor for the synthesis of heterocyclic compounds and biologically active molecules. By incorporating this building block into synthetic pathways, chemists can access a diverse array of heterocyclic scaffolds with potential applications in drug discovery, materials science, and agrochemical development. The versatility and reactivity of 3-(Methoxymethyl)pyrrolidine make it a valuable asset in the toolkit of synthetic chemists seeking to access novel chemical space and functionalized structures.