1H-Pyrrole-2-carboxylic acid, 1-(2-phenylethenyl)-, (Z)-

Base Information

Chemical Name:1H-Pyrrole-2-carboxylic acid, 1-(2-phenylethenyl)-, (Z)-
CAS No.:34600-56-1
Molecular Formula:C₁₃H₁₁NO₂
Molecular Weight:213.236
Hs Code.:
DSSTox Substance ID:DTXSID001200031

Synonyms:SCHEMBL11741711;1H-Pyrrole-2-carboxylic acid, 1-(2-phenylethenyl)-, (Z)-;DTXSID001200031;34600-56-1

Suppliers and Price of 1H-Pyrrole-2-carboxylic acid, 1-(2-phenylethenyl)-, (Z)-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 1H-Pyrrole-2-carboxylic acid, 1-(2-phenylethenyl)-, (Z)-

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:213.078978594
Heavy Atom Count:16
Complexity:269

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C=CN2C=CC=C2C(=O)O
Isomeric SMILES:C1=CC=C(C=C1)/C=C\N2C=CC=C2C(=O)O

Technology Process of 1H-Pyrrole-2-carboxylic acid, 1-(2-phenylethenyl)-, (Z)-

There total 4 articles about 1H-Pyrrole-2-carboxylic acid, 1-(2-phenylethenyl)-, (Z)- 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%

: 34600-57-2
N-(trans-Styryl)pyrrol-2-carbonsaeure

: 34600-56-1
cis-1-Styrylpyrrol-2-carbonsaeure

Guidance literature:: In ethanol; for 5h; Irradiation;
DOI:10.1021/jo00167a016

Reference yield:

: 35566-71-3
3-phenyl-3,4-dihydro-pyrrolo[2,1-c][1,4]oxazin-1-one

: 34600-56-1
cis-1-Styrylpyrrol-2-carbonsaeure

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / potassium tert-butoxide / dimethylformamide / 0.25 h / Ambient temperature

2: 83 percent / aq. ethanol / 5 h / Irradiation

With potassium tert-butylate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jo00167a016