2-Propoxybenzamide

Base Information

Chemical Name:2-Propoxybenzamide
CAS No.:59643-84-4
Molecular Formula:C10H13 N O2
Molecular Weight:179.219
Hs Code.:2924299090
European Community (EC) Number:261-836-1
DSSTox Substance ID:DTXSID30208310
Nikkaji Number:J149.177F
Wikidata:Q83082416
Mol file:59643-84-4.mol

Synonyms:2-propoxybenzamide;59643-84-4;o-Propoxybenzamide;2-n-Propoxybenzamide;BENZAMIDE, o-PROPOXY-;H.P. 206;EINECS 261-836-1;BRN 2966043;2-propoxy-benzamide;SCHEMBL3352936;DTXSID30208310;HLP-206;STL062012;AKOS000504273;LS-27390;CS-0365084;FT-0674085

Suppliers and Price of 2-Propoxybenzamide

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-Propoxybenzamide
250mg
$ 85.00

Aronis compounds
2-propoxybenzamide
5mg
$ 15.00

American Custom Chemicals Corporation
2-PROPOXYBENZAMIDE 98.00%
5G
$ 1767.15

American Custom Chemicals Corporation
2-PROPOXYBENZAMIDE 98.00%
500MG
$ 704.55

Total 9 raw suppliers

Chemical Property of 2-Propoxybenzamide

Chemical Property:

Melting Point:94-96°C
Refractive Index:1.5150 (estimate)
Boiling Point:311.75°C (rough estimate)
PKA:15.61±0.50(Predicted)
PSA：52.32000
Density:1.1248 (rough estimate)
LogP:2.27460
XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:179.094628657
Heavy Atom Count:13
Complexity:170

Purity/Quality:

98%Min ^*data from raw suppliers

2-Propoxybenzamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCOC1=CC=CC=C1C(=O)N
Uses 2-Propoxybenzamide (cas# 59643-84-4) is a compound useful in organic synthesis.

Technology Process of 2-Propoxybenzamide

There total 7 articles about 2-Propoxybenzamide 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: 95.0%

: 106-94-5
propyl bromide

: 65-45-2
salicylamide

: 59643-84-4
2-n-propoxybenzamide

Guidance literature:: With sodium hydroxide; In ethanol; Reflux; Large scale;
DOI:10.1021/acs.oprd.1c00184

Reference yield: 92.0%

: 65-45-2
salicylamide

: 59643-84-4
2-n-propoxybenzamide

Guidance literature:: With sodium hydroxide; In ethanol; for 6h; Reflux;
DOI:10.1016/j.bmc.2015.02.043

Reference yield: 64.0%

: 71-23-8
propan-1-ol

: 4001-73-4
2-Bromobenzamide

: 2-(2-propoxyphenyl)quinazolin-4(3H)-one

: 59643-84-4
2-n-propoxybenzamide

Guidance literature:: With copper(l) iodide; caesium carbonate; at 120 ℃; for 0.166667h; under 9308.91 Torr; Microwave irradiation;
DOI:10.1002/ejoc.201800660