4-iodo-N-methylbenzamide

Base Information

Chemical Name:4-iodo-N-methylbenzamide
CAS No.:89976-43-2
Molecular Formula:C₈H₈INO
Molecular Weight:261.062
Hs Code.:
DSSTox Substance ID:DTXSID301313239
Nikkaji Number:J3.408.004F

Synonyms:4-iodo-N-methylbenzamide;89976-43-2;Benzamide, 4-iodo-N-methyl-;4-Iodo N-methylbenzamide;N-Methyl-4-iodobenzamide;4-iodo-N-methylbenzenamide;SCHEMBL2144483;DTXSID301313239;N-methyl-4-iodobenzoic acid amide;MFCD02945450;AKOS001282975;NCGC00335386-01;CS-16659;CS-0102088;D76275;AB00285917-03;AG-670/15546222;SR-01000229829;SR-01000229829-1;Z30272273

Suppliers and Price of 4-iodo-N-methylbenzamide

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-Iodo-N-methylbenzamide
250mg
$ 55.00

Matrix Scientific
4-Iodo N-methylbenzamide 95%
1g
$ 300.00

Matrix Scientific
4-Iodo N-methylbenzamide 95%
5g
$ 600.00

Matrix Scientific
4-Iodo N-methylbenzamide 95%
10g
$ 800.00

Crysdot
4-Iodo-N-methylbenzamide 95+%
25g
$ 790.00

Crysdot
4-Iodo-N-methylbenzamide 95+%
10g
$ 395.00

Chemenu
4-Iodo-N-methylbenzamide 95%
10g
$ 373.00

Chemenu
4-Iodo-N-methylbenzamide 95%
25g
$ 746.00

Ambeed
4-Iodo-N-methylbenzamide 98%
1g
$ 70.00

Ambeed
4-Iodo-N-methylbenzamide 98%
10g
$ 373.00

Total 8 raw suppliers

Chemical Property of 4-iodo-N-methylbenzamide

Chemical Property:

Storage Temp.:2-8°C(protect from light)
XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:260.96506
Heavy Atom Count:11
Complexity:141

Purity/Quality:

99% ^*data from raw suppliers

4-Iodo-N-methylbenzamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CNC(=O)C1=CC=C(C=C1)I

Technology Process of 4-iodo-N-methylbenzamide

There total 6 articles about 4-iodo-N-methylbenzamide 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: 92.0%

: 619-58-9
4-iodobenzoic acid

: 74-89-5
methylamine

: 89976-43-2
4-iodo-N-methylbenzenamide

Guidance literature:: 4-iodobenzoic acid; With thionyl chloride; at 20 ℃; for 0.5h;

methylamine; In water; at 20 ℃; for 2h;
DOI:10.1016/j.jorganchem.2004.01.027

Reference yield: 27.0%

: 421-20-5
Methyl fluorosulfonate

: 3058-39-7
4-iodobenzonitrile

: 89976-43-2
4-iodo-N-methylbenzenamide

Guidance literature:: at 20 ℃; for 70h;

Reference yield:

: 74-89-5
methylamine

: 1711-02-0
4-iodobenzoic acid chloride

: 89976-43-2
4-iodo-N-methylbenzenamide

Guidance literature:: With triethylamine; In methanol; diethyl ether; at 20 ℃; for 1h; Inert atmosphere; Schlenk technique;
DOI:10.1021/ja400020e