N,N-Diisopropyldichloroacetamide

Base Information

Chemical Name:N,N-Diisopropyldichloroacetamide
CAS No.:5326-93-2
Molecular Formula:C8H15Cl2NO
Molecular Weight:212.1168
Hs Code.:2924199090
NSC Number:4086
DSSTox Substance ID:DTXSID6063777
Nikkaji Number:J421.756J
Wikidata:Q81991002
Mol file:5326-93-2.mol

Synonyms:N,N-Diisopropyldichloroacetamide;5326-93-2;Acetamide, 2,2-dichloro-N,N-bis(1-methylethyl)-;2,2-Dichloro-N,N-bis(1-methylethyl)acetamide;NSC 4086;AI3-32495;2,N-bis(1-methylethyl)acetamide;NSC4086;C8H15Cl2NO;SCHEMBL7129705;DTXSID6063777;NSC-4086;AKOS003868006;2,2-dichloro-N,N-bis(propan-2-yl)acetamide;Acetamide,2-dichloro-N,N-bis(1-methylethyl)-;ACETAMIDE,2,2-DICHLORO-N,N-BIS(1-METHYLETHYL)-

Suppliers and Price of N,N-Diisopropyldichloroacetamide

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

American Custom Chemicals Corporation
ACETAMIDE,2,2-DICHLORO-N,N-BIS(1-METHYLETHYL)- 95.00%
5MG
$ 495.69

Total 6 raw suppliers

Chemical Property of N,N-Diisopropyldichloroacetamide

Chemical Property:

Vapor Pressure:0.0316mmHg at 25°C
Boiling Point:243.7°Cat760mmHg
Flash Point:101.2°C
PSA：20.31000
Density:1.123g/cm³
LogP:2.43550
XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:211.0530695
Heavy Atom Count:12
Complexity:149

Purity/Quality:

99% ^*data from raw suppliers

ACETAMIDE,2,2-DICHLORO-N,N-BIS(1-METHYLETHYL)- 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)N(C(C)C)C(=O)C(Cl)Cl

Technology Process of N,N-Diisopropyldichloroacetamide

There total 6 articles about N,N-Diisopropyldichloroacetamide 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: 90.0%

: 79-36-7
dichloroacethyl chloride

: 108-18-9
diisopropylamine

: 5326-93-2
N,N-diisopropyl-2,2-dichloroacetamide

Guidance literature:: In dichloromethane; for 5h; Heating;
DOI:10.1021/jo701417z

Reference yield: 41.0%

: 7087-68-5
N-ethyl-N,N-diisopropylamine

: 5326-93-2
N,N-diisopropyl-2,2-dichloroacetamide

Guidance literature:: N-ethyl-N,N-diisopropylamine; With 1,4-diaza-bicyclo[2.2.2]octane; disulfur dichloride; In chloroform; at 20 ℃; for 72h;

With formic acid; In chloroform; for 1.5h; Heating;
DOI:10.1070/MC2001v011n05ABEH001504

Reference yield: 34.0%

: 96-79-7
(2-chloroethyl)-diisopropylamine

: 5326-93-2
N,N-diisopropyl-2,2-dichloroacetamide

: 406913-23-3
5-chloro-4-[(2-chloro-ethyl)-isopropyl-amino]-[1,2]dithiol-3-one

Guidance literature:: (2-chloroethyl)-diisopropylamine; With 1,4-diaza-bicyclo[2.2.2]octane; disulfur dichloride; In chloroform; at 0 ℃; for 72h;

With formic acid; In chloroform; for 1.5h; Heating;
DOI:10.1070/MC2001v011n05ABEH001504