1. Home
  2. (3R)-3-(3,4-dichlorophenyl)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)-

(3R)-3-(3,4-dichlorophenyl)pyrrolidine

Clc1ccc(cc1Cl)C1CNCC1 Request for Quotation
Chemical Name: (3R)-3-(3,4-dichlorophenyl)pyrrolidine
CAS Number: 1092108-78-5
Product Number: AG00966V(AGN-PC-0J3ZMR)
Synonyms:
MDL No:
Molecular Formula: C10H11Cl2N
Molecular Weight: 216.1070

Identification/Properties

Computed Properties
Molecular Weight:
216.105g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
215.027g/mol
Monoisotopic Mass:
215.027g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
174
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


3-(3,4-Dichlorophenyl)pyrrolidine is a versatile compound that finds its application in various chemical synthesis processes. This compound serves as a key building block in the creation of bioactive molecules, pharmaceuticals, and agrochemicals. Due to its unique structure, 3-(3,4-Dichlorophenyl)pyrrolidine facilitates the formation of complex molecular structures with enhanced biological activities. Its use in the synthesis of drug candidates and other valuable compounds highlights its importance in modern organic chemistry. Furthermore, the incorporation of 3-(3,4-Dichlorophenyl)pyrrolidine in synthetic pathways offers chemists a powerful tool for accessing diverse chemical space and developing novel compounds with potential applications in various industries.