1H-Pyrrole, 2-(3-chlorophenyl)-

Base Information

Chemical Name:1H-Pyrrole, 2-(3-chlorophenyl)-
CAS No.:115464-89-6
Molecular Formula:C10H8ClN
Molecular Weight:177.633
Hs Code.:
NSC Number:116793
DSSTox Substance ID:DTXSID00297599
Nikkaji Number:J2.100.940G
Wikidata:Q82038780
Mol file:115464-89-6.mol

Synonyms:115464-89-6;2-(3-chlorophenyl)pyrrole;2-(3-Chlorophenyl)-1H-pyrrole;1H-Pyrrole, 2-(3-chlorophenyl)-;NSC116793;SCHEMBL237434;DTXSID00297599;AC3028;MFCD08689215;NSC-116793;SY129933;A927170

Suppliers and Price of 1H-Pyrrole, 2-(3-chlorophenyl)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of 1H-Pyrrole, 2-(3-chlorophenyl)-

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:177.0345270
Heavy Atom Count:12
Complexity:149

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC(=C1)Cl)C2=CC=CN2

Technology Process of 1H-Pyrrole, 2-(3-chlorophenyl)-

There total 10 articles about 1H-Pyrrole, 2-(3-chlorophenyl)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 80.0%

: 115464-89-6
2-(3-chlorophenyl)-1H-pyrrole

Guidance literature:: With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate; In ethanol; water; toluene; at 110 ℃; for 12h; Sealed tube; Inert atmosphere;

With potassium carbonate; In methanol; for 12h; Inert atmosphere; Reflux;

Reference yield: 61.0%

: 109-97-7,30604-81-0
pyrrole

: 63503-60-6
3-chlorophenylboronic acid

: 115464-89-6
2-(3-chlorophenyl)-1H-pyrrole

Guidance literature:: With iron(II) oxalate dihydrate; 3,6,9,15-tetraazabicyclo[9.3.1]pentadeca-1⁽¹⁴⁾,11⁽¹⁵⁾,12-triene; at 130 ℃; for 10h; regioselective reaction;
DOI:10.1021/ol100838m

Reference yield: 58.0%

: trans-2-(tributylstannyl)-N,N-dibenzylcyclopropylamine

: 766-84-7
3-chloro-benzonitrile

: 115464-89-6
2-(3-chlorophenyl)-1H-pyrrole

Guidance literature:: trans-2-(tributylstannyl)-N,N-dibenzylcyclopropylamine; 3-chloro-benzonitrile; With n-butyllithium; In tetrahydrofuran; hexane; at -30 - 0 ℃; for 2.5h;

With acetic acid; In tetrahydrofuran; hexane;
DOI:10.1055/s-2006-950410