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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-Methylpyrrolidine-2-carboxylic acid hydrochloride

CN1CCCC1C(=O)O.Cl Request for Quotation
Chemical Name: 1-Methylpyrrolidine-2-carboxylic acid hydrochloride
CAS Number: 30727-22-1
Product Number: AG00312C(AGN-PC-0WAMOI)
Synonyms:
MDL No: MFCD18071558
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:
1
Exact Mass:
165.056g/mol
Monoisotopic Mass:
165.056g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
124
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Methylpyrrolidine-2-carboxylic acid hydrochloride, also known as $name$, is a versatile compound widely employed in chemical synthesis processes. This powerful acid derivative serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique chemical properties make it an invaluable tool in the development of novel drug candidates and fine chemicals. In organic synthesis, $name$ acts as a key intermediate, facilitating the formation of complex molecular structures while offering precise control over reaction pathways. Researchers and chemists rely on its reactivity and compatibility with a diverse range of reagents to design efficient synthetic routes and achieve high yields of target compounds. The utilization of 1-Methylpyrrolidine-2-carboxylic acid hydrochloride in chemical synthesis enables the rapid, scalable production of valuable molecules with enhanced purity and selectivity, driving innovation and advancement in various industries.