(1H-Indole-2-ylmethyl)diethylamine

Base Information

Chemical Name:(1H-Indole-2-ylmethyl)diethylamine
CAS No.:3978-16-3
Molecular Formula:C11H14N2
Molecular Weight:174.24226
Hs Code.:
Nikkaji Number:J2.315.363G
Mol file:3978-16-3.mol

Synonyms:N-((1H-Indol-2-yl)methyl)-N-ethylethanamine;Indole 2-N,N-Diethylmethylamine-13C;N-ethyl-N-(1H-indol-2-ylmethyl)ethanamine;(1H-Indole-2-ylmethyl)diethylamine;2-diethylaminomethylindole;SCHEMBL8574842

Suppliers and Price of (1H-Indole-2-ylmethyl)diethylamine

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
2-[(Dimethylamino)methyl]indole
100mg
$ 140.00

American Custom Chemicals Corporation
N,N-DIMETHYL-1H-INDOLE-2-METHANAMINE 95.00%
5MG
$ 505.77

Total 6 raw suppliers

Chemical Property of (1H-Indole-2-ylmethyl)diethylamine

Chemical Property:

Vapor Pressure:0.00168mmHg at 25°C
Boiling Point:293.9°C at 760 mmHg
Flash Point:131.5°C
PSA：19.03000
Density:1.099g/cm³
LogP:2.22950
Storage Temp.:Refrigerator
Solubility.:Chloroform (Slightly), Methanol (Very Slightly)
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:202.146998583
Heavy Atom Count:15
Complexity:189

Purity/Quality:

96% ^*data from raw suppliers

2-[(Dimethylamino)methyl]indole ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN(CC)CC1=CC2=CC=CC=C2N1
Uses 2-[(Dimethylamino)methyl]indole (cas# 3978-16-3) is a compound useful in organic synthesis.

Technology Process of (1H-Indole-2-ylmethyl)diethylamine

There total 11 articles about (1H-Indole-2-ylmethyl)diethylamine 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: 97.0%

: 148564-88-9
2,2,2-trifluoro-N-(2-(3-hydroxyprop-1-ynyl)phenyl)acetamide

: 109-89-7
diethylamine

: 3978-16-3
N-((1H-indol-2-yl)methyl)-N-ethylethanamine

Guidance literature:: With copper(l) iodide; potassium carbonate; In acetonitrile; at 80 ℃; for 1h; Reagent/catalyst;
DOI:10.1002/adsc.201400881

Reference yield: 82.0%

: 41979-44-6
N,N-diethyl-1H-indole-2-carboxamide

: 3978-16-3
N-((1H-indol-2-yl)methyl)-N-ethylethanamine

Guidance literature:: With bis(2-chlorophenyl)borinic acid; phenylsilane; In toluene; at 65 ℃; for 12h; Sealed tube; Inert atmosphere;
DOI:10.1002/chem.201604802

Reference yield: 69.0%

: 148564-88-9
2,2,2-trifluoro-N-(2-(3-hydroxyprop-1-ynyl)phenyl)acetamide

: 109-89-7
diethylamine

: 24621-70-3
2-(hydroxymethyl)indole

: 3978-16-3
N-((1H-indol-2-yl)methyl)-N-ethylethanamine

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; In N,N-dimethyl-formamide; at 80 ℃; for 1.5h; Reagent/catalyst; Solvent; Time; Temperature; Inert atmosphere;
DOI:10.1021/jo401456x