2-[(Ethylamino)methyl]-4-aminophenol Dihydrochloride

Base Information

Chemical Name:2-[(Ethylamino)methyl]-4-aminophenol Dihydrochloride
CAS No.:86177-06-2
Molecular Formula:C9H16Cl2N2O
Molecular Weight:239.145
Hs Code.:
Mol file:86177-06-2.mol

Synonyms:4-AMino-2-[(ethylaMino)Methyl]phenol Dihydrochloride

Suppliers and Price of 2-[(Ethylamino)methyl]-4-aminophenol Dihydrochloride

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
2-[(Ethylamino)methyl]-4-aminophenolDihydrochloride
1g
$ 1055.00

Medical Isotopes, Inc.
2-[(Ethylamino)methyl]-4-aminophenolDiHCl
100 mg
$ 870.00

Medical Isotopes, Inc.
2-[(Ethylamino)methyl]-4-aminophenolDiHCl
0.5 g
$ 1960.00

American Custom Chemicals Corporation
2-[(ETHYLAMINO)METHYL]-4-AMINOPHENOL DIHYDROCHLORIDE 95.00%
1G
$ 1686.30

American Custom Chemicals Corporation
2-[(ETHYLAMINO)METHYL]-4-AMINOPHENOL DIHYDROCHLORIDE 95.00%
100MG
$ 716.10

Total 4 raw suppliers

Chemical Property of 2-[(Ethylamino)methyl]-4-aminophenol Dihydrochloride

Chemical Property:

PSA：58.28000
LogP:3.66000

Purity/Quality:

99% ^*data from raw suppliers

2-[(Ethylamino)methyl]-4-aminophenolDihydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 2-[(Ethylamino)methyl]-4-aminophenol Dihydrochloride is Used in the synthesis of N-[4-[[4-alkoxy-3-[(dialkylamino)methyl]phenyl]amino]-2-pyrimidinyl]-N'-phenylguanidines with antifilarial activity. Used in the synthesis of N-[4-[[4-alkoxy-3-[(dialkylamino)methyl]phenyl]amino]-2-pyrimidinyl]-N''-phenylguanidines with antifilarial activity.

Technology Process of 2-[(Ethylamino)methyl]-4-aminophenol Dihydrochloride

There total 4 articles about 2-[(Ethylamino)methyl]-4-aminophenol Dihydrochloride 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: 94.0%

: 71130-60-4
2‐(ethylamino)methyl‐4‐nitrophenol

: 86177-06-2
4‐amino‐2‐((ethylamino)methyl)phenol dihydrochloride

Guidance literature:: With hydrogenchloride; hydrogen; nickel; In isopropyl alcohol; for 0.5h; under 2637.5 Torr;
DOI:10.1021/jm00363a010

Reference yield:

: 2973-19-5
2-hydroxy-5-nitrobenzyl chloride

: 86177-06-2
4‐amino‐2‐((ethylamino)methyl)phenol dihydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / tetrahydrofuran; H₂O / 20 h

2: 94 percent / H₂, HCl / Raney nickel / propan-2-ol / 0.5 h / 2637.5 Torr

With hydrogenchloride; hydrogen; nickel; In tetrahydrofuran; water; isopropyl alcohol;
DOI:10.1021/jm00363a010

Reference yield:

: 97-51-8
5-Nitrosalicylaldehyde

: 86177-06-2
4‐amino‐2‐((ethylamino)methyl)phenol dihydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: tetrahydrofuran / 3 h / Reflux

2: sodium tetrahydroborate; sodium hydroxide / water; methanol / 20 °C

3: hydrogenchloride; palladium 10% on activated carbon; hydrogen / water / 20 °C / 2327.23 - 2585.81 Torr

With hydrogenchloride; sodium tetrahydroborate; palladium 10% on activated carbon; hydrogen; sodium hydroxide; In tetrahydrofuran; methanol; water;
DOI:10.1002/jlcr.3721