1H-Pyrrole-2-carboxaldehyde, 3,4-diphenyl-

Base Information

Chemical Name:1H-Pyrrole-2-carboxaldehyde, 3,4-diphenyl-
CAS No.:105508-07-4
Molecular Formula:C17H13NO
Molecular Weight:247.296
Hs Code.:
DSSTox Substance ID:DTXSID00450162
Wikidata:Q82269755
Mol file:105508-07-4.mol

Synonyms:1H-Pyrrole-2-carboxaldehyde, 3,4-diphenyl-;105508-07-4;2-formyl-3,4-diphenylpyrrole;SCHEMBL5534778;DTXSID00450162

Suppliers and Price of 1H-Pyrrole-2-carboxaldehyde, 3,4-diphenyl-

Supply Marketing:

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

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Chemical Property of 1H-Pyrrole-2-carboxaldehyde, 3,4-diphenyl-

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:247.099714038
Heavy Atom Count:19
Complexity:292

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CNC(=C2C3=CC=CC=C3)C=O

Technology Process of 1H-Pyrrole-2-carboxaldehyde, 3,4-diphenyl-

There total 12 articles about 1H-Pyrrole-2-carboxaldehyde, 3,4-diphenyl- 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: 83.0%

: 1632-48-0
3,4-diphenyl-1H-pyrrole

: 68-12-2,33513-42-7
N,N-dimethyl-formamide

: 105508-07-4
3,4-diphenyl-1H-pyrrole-2-carboxaldehyde

Guidance literature:: With trichlorophosphate; at 70 ℃; for 1h;
DOI:10.1002/ardp.19863190812

Reference yield: 72.0%

: 910032-54-1
N-methoxy-N-methyl-3,4-diphenyl-1H-pyrrole-2-carboxamide

: 105508-07-4
3,4-diphenyl-1H-pyrrole-2-carboxaldehyde

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃;
DOI:10.1021/jo061043m

Reference yield:

: 1215-07-2
(E)-(1-nitroethene-1,2-diyl)dibenzene

: 105508-07-4
3,4-diphenyl-1H-pyrrole-2-carboxaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / DBU / tetrahydrofuran / 4.5 h / 0 - 20 °C

2: 72 percent / LiAlH₄ / tetrahydrofuran / 0 °C

With lithium aluminium tetrahydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran;
DOI:10.1021/jo061043m