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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-Pyrrolidinecarboxylic acid, methyl ester, hydrochloride

COC(=O)C1CNCC1.Cl Request for Quotation
Chemical Name: 3-Pyrrolidinecarboxylic acid, methyl ester, hydrochloride
CAS Number: 198959-37-4
Product Number: AG002BU9(AGN-PC-02A1VG)
Synonyms:
MDL No: MFCD08436169
Molecular Formula: C6H12ClNO2
Molecular Weight: 165.6180

Identification/Properties

Computed Properties
Molecular Weight:
165.617g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
165.056g/mol
Monoisotopic Mass:
165.056g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
114
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 3-pyrrolidinecarboxylate hydrochloride is a versatile compound commonly employed in chemical synthesis as a key building block for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Due to its unique structural features and reactivity, this compound serves as an essential intermediate in the synthesis of numerous complex organic molecules. Its application in chemical transformations such as esterification, amidation, and ring formation reactions makes it a valuable tool for organic chemists seeking to access diverse molecular scaffolds. Whether used in the development of new drug candidates or the creation of specialized materials, Methyl 3-pyrrolidinecarboxylate hydrochloride plays a crucial role in advancing the field of synthetic chemistry.