BENZOPHENONE-4-IODOACETAMIDE

Base Information

Chemical Name:BENZOPHENONE-4-IODOACETAMIDE
CAS No.:76809-63-7
Molecular Formula:C15H12INO2
Molecular Weight:365.17
Hs Code.:2924299090
Mol file:76809-63-7.mol

Synonyms:BENZOPHENONE-4-IODOACETAMIDE;BENZOIN;4-(N-Iodoacetamide)benzophenone;N-(4-Benzoylphenyl)-2-iodoacetaMide

Suppliers and Price of BENZOPHENONE-4-IODOACETAMIDE

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
4-(N-Iodoacetamide)benzophenone
25mg
$ 185.00

TRC
4-(N-Iodoacetamide)benzophenone
10mg
$ 105.00

TRC
4-(N-Iodoacetamide)benzophenone
250mg
$ 1335.00

TRC
4-(N-Iodoacetamide)benzophenone
100mg
$ 700.00

Medical Isotopes, Inc.
4-(N-Iodoacetamide)benzophenone
25 mg
$ 650.00

American Custom Chemicals Corporation
4-(N-IODOACETAMIDE)BENZOPHENONE 95.00%
5MG
$ 497.55

Total 15 raw suppliers

Chemical Property of BENZOPHENONE-4-IODOACETAMIDE

Chemical Property:

Vapor Pressure:9.67E-11mmHg at 25°C
Melting Point:168-169 °C
Refractive Index:1.683
Boiling Point:515.6 °C at 760 mmHg
Flash Point:265.6 °C
PSA：46.17000
Density:1.663 g/cm³
LogP:3.36410
Storage Temp.:-20°C Freezer
Solubility.:DMSO (Slightly), Methanol (Slightly)

Purity/Quality:

98%Min ^*data from raw suppliers

4-(N-Iodoacetamide)benzophenone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses A sulfhydryl reactive heterobifunctional photocrosslinking reagent. A sulfhydryl reactive heterobifunctional photocrosslinking reagent

Technology Process of BENZOPHENONE-4-IODOACETAMIDE

There total 2 articles about BENZOPHENONE-4-IODOACETAMIDE 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%

: 70110-37-1
2-chloro-N-(4-aminobenzophenone)acetamide

: 76809-63-7
N-(4-Benzoyl-phenyl)-2-iodo-acetamide

Guidance literature:: With sodium iodide;
DOI:10.1248/cpb.28.2720

Reference yield:

: 1137-41-3,444317-48-0
(4-aminophenyl)(phenyl)methanone

: 76809-63-7
N-(4-Benzoyl-phenyl)-2-iodo-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent

2: 95 percent / NaI

With sodium iodide;
DOI:10.1248/cpb.28.2720