Propanoic acid, 2,2-dimethyl-, 2-(dichloroamino)-2-methylpropyl ester

Base Information

Chemical Name:Propanoic acid, 2,2-dimethyl-, 2-(dichloroamino)-2-methylpropyl ester
CAS No.:61542-21-0
Molecular Formula:C9H17Cl2NO2
Molecular Weight:242.1428
Hs Code.:
DSSTox Substance ID:DTXSID90210535

Synonyms:Propanoic acid, 2,2-dimethyl-, 2-(dichloroamino)-2-methylpropyl ester;61542-21-0;SCHEMBL4452340;DTXSID90210535

Suppliers and Price of Propanoic acid, 2,2-dimethyl-, 2-(dichloroamino)-2-methylpropyl ester

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Propanoic acid, 2,2-dimethyl-, 2-(dichloroamino)-2-methylpropyl ester

Chemical Property:

Vapor Pressure:0.00525mmHg at 25°C
Boiling Point:274.9°Cat760mmHg
Flash Point:120.1°C
Density:1.149g/cm³
XLogP3:2.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:241.0636342
Heavy Atom Count:14
Complexity:209

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Propanoic acid, 2,2-dimethyl-, 2-(dichloroamino)-2-methylpropyl ester

There total 3 articles about Propanoic acid, 2,2-dimethyl-, 2-(dichloroamino)-2-methylpropyl ester 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:

: 90949-59-0
2-tert-butyl-4,4-dimethyl-4,5-dihydrooxazole

: 61542-21-0
2-N,N-Dichloroamino-2-methyl-1-propyl 2,2-dimethylpropionate

Guidance literature:: Multi-step reaction with 2 steps

1: aq. HCl / tetrahydrofuran

2: NaOCl

With hydrogenchloride; sodium hypochlorite; In tetrahydrofuran;
DOI:10.1002/jps.2600651210