(3S,4R)-4-(Pyridin-4-yl)pyrrolidine-3-carboxylic acid dihydrochloride|1049740-23-9,AngeneChemical

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

(3S,4R)-4-(Pyridin-4-yl)pyrrolidine-3-carboxylic acid dihydrochloride

Request for Quotation

Chemical Name:	(3S,4R)-4-(Pyridin-4-yl)pyrrolidine-3-carboxylic acid dihydrochloride
CAS Number:	1049740-23-9
Product Number:	AG008XL4(AGN-PC-0WAGE7)
Synonyms:
MDL No:
Molecular Formula:	C10H14Cl2N2O2
Molecular Weight:	265.13636

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
Customer Feedback

Identification/Properties

Safety Information

GHS Pictogram:

N/A

Signal Word:

UN#:

Hazard Statements:

Precautionary Statements:

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

Request for Quotation

Quantity Required:*

Company Name:

Contact Person:*

Email:*

Tel:*

Country:*

Others:(Optional)

Verification Code:

Customer Feedback

Chemical Structure

The (3S,4R)-4-(Pyridin-4-yl)pyrrolidine-3-carboxylic acid dihydrochloride is a versatile compound widely used in chemical synthesis as a valuable building block. Its unique structure with a pyrrolidine and pyridine ring confers specific reactivity and functionality that are highly beneficial in organic chemistry transformations.In chemical synthesis, this compound serves as a key intermediate for the construction of complex molecules with desired chirality. Its presence allows for the introduction of diverse functional groups and motifs through various reactions such as nucleophilic substitutions, cross-coupling reactions, and ring-closure reactions.Furthermore, the dihydrochloride salt form of this compound enhances its solubility and stability, making it easier to handle and manipulate during synthesis processes. Its controlled stereochemistry and regioselectivity make it a preferred reagent for the preparation of biologically-active compounds, pharmaceutical intermediates, and agrochemicals with high purity and efficiency.