1H-Pyrrole-1-acetic acid, 3-(ethoxycarbonyl)-2-methyl-5-phenyl-

Base Information

Chemical Name:1H-Pyrrole-1-acetic acid, 3-(ethoxycarbonyl)-2-methyl-5-phenyl-
CAS No.:679797-47-8
Molecular Formula:C₁₆H₁₇NO₄
Molecular Weight:287.315
Hs Code.:
DSSTox Substance ID:DTXSID50390509
Wikidata:Q27195726
ChEMBL ID:CHEMBL1423539

Synonyms:679797-47-8;1H-Pyrrole-1-acetic acid, 3-(ethoxycarbonyl)-2-methyl-5-phenyl-;2-(3-ethoxycarbonyl-2-methyl-5-phenylpyrrol-1-yl)acetic acid;[3-(ethoxycarbonyl)-2-methyl-5-phenyl-1H-pyrrol-1-yl]acetic acid;2-(3-(Ethoxycarbonyl)-2-methyl-5-phenyl-1H-pyrrol-1-yl)acetic acid;MLS000047618;2-[3-(ethoxycarbonyl)-2-methyl-5-phenyl-1H-pyrrol-1-yl]acetic acid;HMS2289P07;ChemDiv3_014366;CHEMBL1423539;DTXSID50390509;CHEBI:114327;HMS1513M22;AKOS000266720;IDI1_030164;SMR000033629;CS-0364435;SR-01000147444;SR-01000147444-1;Q27195726;2-(3-ethoxycarbonyl-2-methyl-5-phenyl-1-pyrrolyl)acetic acid

Suppliers and Price of 1H-Pyrrole-1-acetic acid, 3-(ethoxycarbonyl)-2-methyl-5-phenyl-

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 3 raw suppliers

Chemical Property of 1H-Pyrrole-1-acetic acid, 3-(ethoxycarbonyl)-2-methyl-5-phenyl-

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:287.11575802
Heavy Atom Count:21
Complexity:379

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)C1=C(N(C(=C1)C2=CC=CC=C2)CC(=O)O)C

Technology Process of 1H-Pyrrole-1-acetic acid, 3-(ethoxycarbonyl)-2-methyl-5-phenyl-

There total 1 articles about 1H-Pyrrole-1-acetic acid, 3-(ethoxycarbonyl)-2-methyl-5-phenyl- 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:

: 89201-10-5
α-Phenacyl-acetessigsaeure-aethylester

: 56-40-6,18875-39-3,25718-94-9
glycine

: 679797-47-8
(3-ethoxycarbonyl-2-methyl-5-phenyl-pyrrol-1-yl)-acetic acid

Guidance literature:: With acetic acid;

Reference yield:

: 679797-47-8
(3-ethoxycarbonyl-2-methyl-5-phenyl-pyrrol-1-yl)-acetic acid

: 541-41-3
chloroformic acid ethyl ester

: 1-(2-ethoxycarbonyloxy-2-oxo-ethyl)-2-methyl-5-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester

Guidance literature:: With triethylamine; In dichloromethane; at -20 ℃; for 0.333333h;

Reference yield:

: 679797-47-8
(3-ethoxycarbonyl-2-methyl-5-phenyl-pyrrol-1-yl)-acetic acid

: 3-[(acetyloxy)methyl]-7-({2-[3-(ethoxycarbonyl)-2-methyl-5-phenyl-1H-1-pyrrolyl]acetyl}amino)-6-oxo-7,7a-dihydro-2H,6H-aceto[2,1-b][1,3]thiazine-4-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / CH₂Cl₂ / 0.33 h / -20 °C

2: 71 percent / CH₂Cl₂ / 4 h / -20 - 20 °C

With triethylamine; In dichloromethane;