1H-indene-3-carboxamide

Base Information

Chemical Name:1H-indene-3-carboxamide
CAS No.:74844-01-2
Molecular Formula:C₁₀H₉NO
Molecular Weight:159.188
Hs Code.:
DSSTox Substance ID:DTXSID70372428
Wikidata:Q82160134
Mol file:74844-01-2.mol

Synonyms:1H-indene-3-carboxamide;74844-01-2;3H-indene-1-carboxamide;Maybridge3_006867;SCHEMBL4527060;1H-Indene-3-carboxamide(9ci);DTXSID70372428;CHEBI:190654;HMS1450I03;CCG-46145;AKOS006278960;IDI1_018254;SR-01000635860-1

Suppliers and Price of 1H-indene-3-carboxamide

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

American Custom Chemicals Corporation
1H-INDENE-3-CARBOXAMIDE 95.00%
5MG
$ 498.50

Total 1 raw suppliers

Chemical Property of 1H-indene-3-carboxamide

Chemical Property:

PSA：44.08000
LogP:2.26110
XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:159.068413911
Heavy Atom Count:12
Complexity:232

Purity/Quality:: 1H-INDENE-3-CARBOXAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C=C(C2=CC=CC=C21)C(=O)N

Technology Process of 1H-indene-3-carboxamide

There total 3 articles about 1H-indene-3-carboxamide 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:

: 14209-41-7
3H-indene-1-carboxylic acid

: 74844-01-2
1H-indene-3-carboxamide

Guidance literature:: With ammonium hydroxide; thionyl chloride; Yield given. Multistep reaction; 1.) benzene, reflux, 2 h; 2.) -10 deg C, 1 h;
DOI:10.1021/jo01311a003