4-(chloromethyl)-N,N-dimethylaniline hydrochloride

Base Information

Chemical Name:4-(chloromethyl)-N,N-dimethylaniline hydrochloride
CAS No.:1703-47-5
Molecular Formula:C₉H₁₂ClN*ClH
Molecular Weight:206.115
Hs Code.:
European Community (EC) Number:860-154-7

Synonyms:4-(chloromethyl)-N,N-dimethylaniline hydrochloride;1703-47-5;4-(chloromethyl)-N,N-dimethylaniline;hydrochloride;SCHEMBL8655320;VORNGBNHDONIJP-UHFFFAOYSA-N;BAA70347;4-dimethylaminobenzylchloride hydrochloride;CS-0250804;EN300-52279;4-(chloromethyl)-N,N-dimethylanilinehydrochloride

Suppliers and Price of 4-(chloromethyl)-N,N-dimethylaniline hydrochloride

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

Total 5 raw suppliers

Chemical Property of 4-(chloromethyl)-N,N-dimethylaniline hydrochloride

Chemical Property:

Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:205.0425048
Heavy Atom Count:12
Complexity:106

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CN(C)C1=CC=C(C=C1)CCl.Cl

Technology Process of 4-(chloromethyl)-N,N-dimethylaniline hydrochloride

There total 3 articles about 4-(chloromethyl)-N,N-dimethylaniline hydrochloride 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: 96.0%

: 1703-46-4
N,N-dimethyl-4-hydroxymethylaniline

: 1703-47-5
p-dimethylaminobenzyl chloride hydrochloride

Guidance literature:: With hydrogenchloride; at 100 ℃; for 15h;

Reference yield:

: 100-10-7
4-dimethylamino-benzaldehyde

: 1703-47-5
p-dimethylaminobenzyl chloride hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: sodium tetrahydroborate / ethanol / 12 h / 20 °C

2: thionyl chloride / dichloromethane / 12 h / 20 °C

With sodium tetrahydroborate; thionyl chloride; In ethanol; dichloromethane;
DOI:10.1021/jacs.1c11503

Reference yield:

: 121-69-7,77733-26-7
N,N-dimethyl-aniline

: 1703-47-5
p-dimethylaminobenzyl chloride hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: concentrated hydrochloric acid

2: hydrochloric acid / 100 °C

With hydrogenchloride;