2-(2-Iodo-benzylamino)-ethanol

Base Information

Chemical Name:2-(2-Iodo-benzylamino)-ethanol
CAS No.:251326-33-7
Molecular Formula:C₉H₁₂INO
Molecular Weight:277.105
Hs Code.:
DSSTox Substance ID:DTXSID301283294
Mol file:251326-33-7.mol

Synonyms:2-(2-Iodo-benzylamino)-ethanol;251326-33-7;2-((2-Iodobenzyl)amino)ethanol;DTXSID301283294;BKA32633;2-[(2-iodophenyl)methylamino]ethanol;2-[[(2-Iodophenyl)methyl]amino]ethanol;AM100572

Suppliers and Price of 2-(2-Iodo-benzylamino)-ethanol

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

Crysdot
2-((2-Iodobenzyl)amino)ethanol 97%
1g
$ 970.00

Total 1 raw suppliers

Chemical Property of 2-(2-Iodo-benzylamino)-ethanol

Chemical Property:

XLogP3:1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:276.99636
Heavy Atom Count:12
Complexity:121

Purity/Quality:: 2-((2-Iodobenzyl)amino)ethanol 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C(=C1)CNCCO)I

Technology Process of 2-(2-Iodo-benzylamino)-ethanol

There total 2 articles about 2-(2-Iodo-benzylamino)-ethanol 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: 91.0%

: 26260-02-6
2-iodobenzaldehyde

: 141-43-5
ethanolamine

: 251326-33-7
N-(2-iodobenzyl)-2-aminoethanol

Guidance literature:: With sodium tetrahydroborate; In ethanol;
DOI:10.1016/S0040-4039(99)01344-1

Reference yield:

: 5159-41-1
2-iodobenzyl alcohol

: 251326-33-7
N-(2-iodobenzyl)-2-aminoethanol

Guidance literature:: Multi-step reaction with 2 steps

1: PDC

2: 91 percent / NaBH₄ / ethanol

With sodium tetrahydroborate; dipyridinium dichromate; In ethanol; 1: Dehydrogenation / 2: Condensation;
DOI:10.1016/S0040-4039(99)01344-1