1H-Indole-2-carboxamide, N-(2-(7-methoxy-1-naphthalenyl)ethyl)-

Base Information

Chemical Name:1H-Indole-2-carboxamide, N-(2-(7-methoxy-1-naphthalenyl)ethyl)-
CAS No.:138112-95-5
Molecular Formula:C22H20N2O2
Molecular Weight:344.4064
Hs Code.:
DSSTox Substance ID:DTXSID30160484
Nikkaji Number:J481.060K
Wikidata:Q83028849
ChEMBL ID:CHEMBL37341
Mol file:138112-95-5.mol

Synonyms:N-(2-(7-Methoxynaphth-1-yl)ethyl)indolecarboxamide;1H-Indole-2-carboxamide, N-(2-(7-methoxy-1-naphthalenyl)ethyl)-;CHEMBL37341;N-(2-(7-Methoxy-1-naphthalenyl)ethyl)-1H-indole-2-carboxamide;138112-95-5;N-[2-(7-Methoxy-1-naphthalenyl)ethyl]-1H-indole-2-carboxamide;SCHEMBL9491485;DTXSID30160484;BDBM50037234;LS-82511;1H-Indole-2-carboxylic acid [2-(7-methoxy-naphthalen-1-yl)-ethyl]-amide

Suppliers and Price of 1H-Indole-2-carboxamide, N-(2-(7-methoxy-1-naphthalenyl)ethyl)-

Supply Marketing:

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

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Chemical Property of 1H-Indole-2-carboxamide, N-(2-(7-methoxy-1-naphthalenyl)ethyl)-

Chemical Property:

Vapor Pressure:2.75E-17mmHg at 25°C
Refractive Index:1.687
Boiling Point:659.9°Cat760mmHg
Flash Point:352.9°C
Density:1.24g/cm³
XLogP3:4.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:344.152477885
Heavy Atom Count:26
Complexity:483

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC2=C(C=CC=C2CCNC(=O)C3=CC4=CC=CC=C4N3)C=C1

Technology Process of 1H-Indole-2-carboxamide, N-(2-(7-methoxy-1-naphthalenyl)ethyl)-

There total 6 articles about 1H-Indole-2-carboxamide, N-(2-(7-methoxy-1-naphthalenyl)ethyl)- 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: 87.0%

: 58881-45-1
Indole-2-carbonyl chloride

: 139525-77-2
2-(7-methoxynaphthalen-1-yl)ethanamine hydrochloride

: 138112-95-5
S 20255

Guidance literature:: With potassium carbonate; In chloroform; water; for 0.5h; Ambient temperature;
DOI:10.1021/jm00046a006

Reference yield:

: 6836-22-2
2-(7-methoxynaphthalen-1-yl)acetic acid

: 138112-95-5
S 20255

Guidance literature:: Multi-step reaction with 4 steps

1: thionyl chloride / CHCl₃

2: aq. NH₄OH / diethyl ether / 0 °C

3: AlH₄ / diethyl ether

4: K₂CO₃ / H₂O; CHCl₃ / 0 °C

With ammonium hydroxide; thionyl chloride; potassium carbonate; tetrahydridoaluminate; In diethyl ether; chloroform; water;
DOI:10.1021/jm00086a018

Reference yield:

: 138113-07-2
2-(2-methoxynaphthalen-8-yl)acetamide

: 138112-95-5
S 20255

Guidance literature:: Multi-step reaction with 2 steps

1: AlH₄ / diethyl ether

2: K₂CO₃ / H₂O; CHCl₃ / 0 °C

With potassium carbonate; tetrahydridoaluminate; In diethyl ether; chloroform; water;
DOI:10.1021/jm00086a018