Ethyl 5-(benzyloxy)-1H-indole-2-carboxylate

Base Information

Chemical Name:Ethyl 5-(benzyloxy)-1H-indole-2-carboxylate
CAS No.:37033-95-7
Molecular Formula:C18H17NO3
Molecular Weight:295.338
Hs Code.:29339900
European Community (EC) Number:253-322-0
NSC Number:30931
UNII:U8E35U2DWT
DSSTox Substance ID:DTXSID20190538
Nikkaji Number:J260.724G
Wikidata:Q72472952
ChEMBL ID:CHEMBL4530157
Mol file:37033-95-7.mol

Synonyms:37033-95-7;Ethyl 5-(benzyloxy)-1H-indole-2-carboxylate;Ethyl 5-benzyloxyindole-2-carboxylate;5-Benzyloxy-2-carbethoxyindole;5-Benzyloxyindole-2-carboxylic acid ethyl ester;Ethyl 5-(phenylmethoxy)-1H-indole-2-carboxylate;1H-Indole-2-carboxylic acid, 5-(phenylmethoxy)-, ethyl ester;5-Benzyloxyindole-2-carboxylic acid ethylester;ethyl 5-phenylmethoxy-1H-indole-2-carboxylate;EINECS 253-322-0;NSC-30931;Ethyl 5-(benzyloxy)indole-2-carboxylate;NSC30931;5-BzlO-ICA-OEt;Maybridge1_002130;U8E35U2DWT;5-benzyloxyindole-2-carboxylic acid*ethyl ester C;Oprea1_318854;SCHEMBL710398;CHEMBL4530157;HMS547I18;DTXSID20190538;2-Carbethoxy-5-(benzyloxy)indole;5-(Benzyloxy)-2-carbethoxyindole;AMY31832;MFCD00022702;NSC 30931;STK028593;AKOS001748204;AC-9375;CCG-235244;CS-W009436;AS-47522;A6374;BB 0253718;FT-0620043;FT-0626280;B-2000;F14089;Ethyl 5-(benzyloxy)-1H-indole-2-carboxylate #;5-Benzyloxy-1H-indole-2-carboxylic acid ethyl ester;ethyl 5-[(phenylmethyl)oxy]-1H-indole-2-carboxylate;5-(Benzyloxy)-1H-indole-2-carboxylic acid ethyl ester

Suppliers and Price of Ethyl 5-(benzyloxy)-1H-indole-2-carboxylate

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

TRC
Ethyl5-(Benzyloxy)-1H-indole-2-carboxylate
2.5g
$ 265.00

SynQuest Laboratories
Ethyl 5-(benzyloxy)-1H-indole-2-carboxylate
5 g
$ 208.00

SynQuest Laboratories
Ethyl 5-(benzyloxy)-1H-indole-2-carboxylate
1 g
$ 128.00

Sigma-Aldrich
5-Benzyloxyindole-2-carboxylic acid ethyl ester
10g
$ 242.00

Matrix Scientific
Ethyl 5-(benzyloxy)-1H-indole-2-carboxylate
500mg
$ 126.00

Crysdot
Ethyl5-(benzyloxy)-1H-indole-2-carboxylate 97%
1g
$ 46.00

Crysdot
Ethyl5-(benzyloxy)-1H-indole-2-carboxylate 97%
5g
$ 197.00

Crysdot
Ethyl5-(benzyloxy)-1H-indole-2-carboxylate 97%
25g
$ 807.00

Crysdot
Ethyl5-(benzyloxy)-1H-indole-2-carboxylate 97%
10g
$ 390.00

Chemenu
Ethyl5-(benzyloxy)-1H-indole-2-carboxylate 95%+
10g
$ 365.00

Total 48 raw suppliers

Chemical Property of Ethyl 5-(benzyloxy)-1H-indole-2-carboxylate

Chemical Property:

Vapor Pressure:2E-09mmHg at 25°C
Melting Point:163 °C
Refractive Index:1.633
Boiling Point:481.4 °C at 760 mmHg
PKA:14?+-.0.30(Predicted)
Flash Point:244.9 °C
PSA：51.32000
Density:1.226 g/cm³
LogP:3.92360
Storage Temp.:−20°C
XLogP3:4.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:295.12084340
Heavy Atom Count:22
Complexity:367

Purity/Quality:

99%, ^*data from raw suppliers

Ethyl5-(Benzyloxy)-1H-indole-2-carboxylate ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CCOC(=O)C1=CC2=C(N1)C=CC(=C2)OCC3=CC=CC=C3
Uses Reactant for preparation of indolyl ethanones as indoleamine 2,3-dioxygenase inhibitors 1 Reactant for preparation of histamine H3 receptor inverse agonists 2 Reactant for preparation of PPAR-γ binding agents with potential application to the treatment of osteoporosis 3 Reactant for preparation of Nonpeptide glycoprotein IIB/IIIA inhibitors 4

Technology Process of Ethyl 5-(benzyloxy)-1H-indole-2-carboxylate

There total 7 articles about Ethyl 5-(benzyloxy)-1H-indole-2-carboxylate 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: 72.0%