N-(1-chloro-2-oxo-2-phenylethyl)benzamide

Base Information

Chemical Name:N-(1-chloro-2-oxo-2-phenylethyl)benzamide
CAS No.:41260-69-9
Molecular Formula:C15H12ClNO2
Molecular Weight:273.719
Hs Code.:
DSSTox Substance ID:DTXSID10560706
Mol file:41260-69-9.mol

Synonyms:N-(1-chloro-2-oxo-2-phenylethyl)benzamide;41260-69-9;benzoylamino(chloro)acetophenone;DTXSID10560706;AKOS005135710

Suppliers and Price of N-(1-chloro-2-oxo-2-phenylethyl)benzamide

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
N-(1-Chloro-2-oxo-2-phenylethyl)benzamide
25mg
$ 615.00

TRC
N-(1-Chloro-2-oxo-2-phenylethyl)benzamide
2.5mg
$ 75.00

Total 0 raw suppliers

Chemical Property of N-(1-chloro-2-oxo-2-phenylethyl)benzamide

Chemical Property:

PSA：49.66000
LogP:3.43900
XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:273.0556563
Heavy Atom Count:19
Complexity:320

Purity/Quality:: N-(1-Chloro-2-oxo-2-phenylethyl)benzamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)C(NC(=O)C2=CC=CC=C2)Cl
Uses N-(1-Chloro-2-oxo-2-phenylethyl)benzamide is an amidophenacylating reagent used in various organic reactions, e.g. in the synthesis of thiohydantoin derivatives.

Technology Process of N-(1-chloro-2-oxo-2-phenylethyl)benzamide

There total 1 articles about N-(1-chloro-2-oxo-2-phenylethyl)benzamide 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:

: 41260-69-9
benzoylamino(chloro)acetophenone

Guidance literature:: d. Produkt aus Phenylglyoxal u. Benzamid, SOCl2;

Reference yield: 96.6%

: 41260-69-9
benzoylamino(chloro)acetophenone

: 1450-86-8,133039-82-4
4-mercaptopyrimidine

: N-[2-Oxo-2-phenyl-1-(pyrimidin-4-ylsulfanyl)-ethyl]-benzamide

Guidance literature:: With triethylamine; In acetonitrile; at 20 ℃; for 20h;
DOI:10.1007/BF01171167

Reference yield: 90.0%

: 41260-69-9
benzoylamino(chloro)acetophenone

: 89713-29-1
benzaldehyde 4-p-tolyl-thiosemicarbazone

: 1173295-37-8
C₃₀H₂₄N₄OS

Guidance literature:: benzoylamino(chloro)acetophenone; benzaldehyde 4-p-tolyl-thiosemicarbazone; In tetrahydrofuran; at 20 - 25 ℃; for 24h;

In methanol; for 1h; Reflux;

With sodium hydrogencarbonate; In water;
DOI:10.1134/S1070363208110236