167886-56-8

Basic information

• Product Name: Carbamic acid, [2-(4-chlorophenyl)ethyl]-, 1,1-dimethylethyl ester
• CAS NO: 167886-56-8
• Molecular Formula: C13H18ClNO2
• Molecular Weight: 255.744
• Mol File: 167886-56-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [2-(4-chlorophenyl)ethyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [2-(4-chlorophenyl)ethyl]-, 1,1-dimethylethyl ester(167886-56-8)
• EPA Substance Registry System: Carbamic acid, [2-(4-chlorophenyl)ethyl]-, 1,1-dimethylethyl ester(167886-56-8)

Safety Data

• Hazardous Substances Data: 167886-56-8(Hazardous Substances Data)

Usage

General Description

Carbamic acid, [2-(4-chlorophenyl)ethyl]-, 1,1-dimethylethyl ester is a chemical compound that belongs to the class of carbamic acids and esters. It is commonly used as a pesticide and insecticide, as well as in the manufacturing of certain pharmaceuticals. Carbamic acid, [2-(4-chlorophenyl)ethyl]-, 1,1-dimethylethyl ester is a colorless to light yellow liquid with a faint odor, and it is soluble in organic solvents. It is considered to be moderately toxic and can pose risks to human health and the environment if not handled properly. Due to its potential hazards, it is important to use caution and follow safety guidelines when working with this chemical.

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 156-41-2 4-chlorophenylethylamine 
• 3506-75-0 4-(4-chlorophenyl)butan-2-one 
• 106-46-7 para-dichlorobenzene 
• 71999-74-1 tert-butyl N-(2-chloroethyl)carbamate 
• 637-87-6 1-Chloro-4-iodobenzene 
• 106-39-8 bromochlorobenzene 

Downstream Products

• 1431697-94-7 (±)-8-chloro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride 
• 1226103-88-3 2-chloro-N-[2-(4-chlorophenyl)ethyl]-N-methylacetamide 
• 38171-31-2 N-methyl-2-(4-chlorophenyl)ethylamine 
• 156-41-2 4-chlorophenylethylamine 
• 824430-78-6 (R)-8-chloro-1-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine L-(+)-tartrate 
• 616202-92-7 lorcaserin 
• 846589-98-8 Lorcaserin hydrochloride 
• 824430-78-6 bis((R)-8-chloro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine) L-(+)-tartarate 
• 616201-80-0 (+/-)-Lorcaserin 
• 55121-08-9 1-chloro-3-(2-isocyanatoethyl)benzene 

Relevant articles and documents

Deacetylative Amination of Acetyl Arenes and Alkanes with C-C Bond Cleavage

The Br?nsted acid-catalyzed synthesis of primary amines from acetyl arenes and alkanes with C-C bond cleavage is described. Although the conversion from an acetyl group to amine has traditionally required multiple steps, the method described herein, which uses an oxime reagent as an amino group source, achieves the transformation directly via domino transoximation/Beckmann rearrangement/Pinner reaction. The method was also applied to the synthesis of γ-aminobutyric acids, such as baclophen and rolipram.

Preparation method and use of lorcaserin hydrochloride

The invention provides a preparation method of lorcaserin hydrochloride, wherein the preparation method comprises the synthetic route described in the specification. The preparation method of lorcaserin hydrochloride has the advantages of simpliness, cheap and easily available raw materials, convenient and safe post-processing, and more green and environmental-protection preparation process, and is an economic synthetic method which can be industrialized.

A kind of products and intermediates green card color forest hydrochloride method for the preparation of (by machine translation)

The invention relates to the field of pharmaceutical chemistry, in particular relates to a diet green card color forest hydrochloride method for the preparation of intermediates thereof. The utility model is characterized in that the preparation method comprises: to the chlorobenzene ethylamine as raw materials, after sequentially acidylated protecting amino group, allyl substituted, deprotected, gram alkylate tougheness, split, a green card color forest of the hydrochloric acid salt. green card color forest hydrochloric acid of the present invention and wherein the intermediate preparation method is low in cost, simple in operation, after treatment is convenient, is an economical, can be industrial synthetic method. (by machine translation)