Ethanol, 2-[(4-chloro-2-nitrophenyl)amino]-, 1-methanesulfonate

Base Information

Chemical Name:Ethanol, 2-[(4-chloro-2-nitrophenyl)amino]-, 1-methanesulfonate
CAS No.:100418-32-4
Molecular Formula:C₉H₁₁ClN₂O₅S
Molecular Weight:294.716
Hs Code.:
DSSTox Substance ID:DTXSID601176280

Synonyms:SCHEMBL10802514;DTXSID601176280;Ethanol, 2-[(4-chloro-2-nitrophenyl)amino]-, 1-methanesulfonate;100418-32-4

Suppliers and Price of Ethanol, 2-[(4-chloro-2-nitrophenyl)amino]-, 1-methanesulfonate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Ethanol, 2-[(4-chloro-2-nitrophenyl)amino]-, 1-methanesulfonate

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:294.0077203
Heavy Atom Count:18
Complexity:377

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CS(=O)(=O)OCCNC1=C(C=C(C=C1)Cl)[N+](=O)[O-]

Technology Process of Ethanol, 2-[(4-chloro-2-nitrophenyl)amino]-, 1-methanesulfonate

There total 1 articles about Ethanol, 2-[(4-chloro-2-nitrophenyl)amino]-, 1-methanesulfonate 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: 75.0%

: 59320-13-7
2-(4-chloro-2-nitrophenylamino)ethanol

: 124-63-0
methanesulfonyl chloride

: 100418-32-4
Methanesulfonic acid 2-(4-chloro-2-nitro-phenylamino)-ethyl ester

Guidance literature:: With pyridine; Ambient temperature;
DOI:10.1016/S0040-4020(01)89768-4

Reference yield: 97.0%

: 100418-32-4
Methanesulfonic acid 2-(4-chloro-2-nitro-phenylamino)-ethyl ester

: 333-20-0
potassium thioacyanate

: 100418-42-6
4-Chloro-2-nitro-N-(2-thiocyanatoethyl)aniline

Guidance literature:: Heating;
DOI:10.1016/S0040-4020(01)89768-4

Reference yield:

: 100418-32-4
Methanesulfonic acid 2-(4-chloro-2-nitro-phenylamino)-ethyl ester

: 100417-16-1
3-(2-amino-4-chlorophenyl)-2-iminothiazolidine dihydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: 97 percent / Heating

2: H₂ / 10percent Pd-C / Ambient temperature; normal pressure

3: HCl gas / CH₂Cl₂; methanol

With hydrogenchloride; hydrogen; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1016/S0040-4020(01)89768-4