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2897-83-8

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2897-83-8 Usage

Originator

Alonimide ,ZYF Pharm Chemical

Uses

Sedativehypnotic.

Manufacturing Process

To a stirred mixture of 58.6 g (0.5 M) of phenyl-acetonitrile and 150 g (1.5 M) of ethyl acrylate was carefully added sodium methoxide in small increments (about 0.1 g). The exothermic reaction was controlled by ice bath cooling to keep the reaction mixture at 50°C. When further additions of sodium methoxide were no longer exothermic, the reaction mixture was stirred for one half hour more and the excess ethyl acrylate removed under reduced pressure on a steam bath. The resulting oil was added to 1.500 g of polyphosphoric acid and stirred on a steam bath for three hours. After cooling to about 50°C, 0.5 liter of chloroform was added followed by additions of crushed ice until the aqueous phase was free flowing. The chloroform layer was separated and combined with three 150 ml chloroform extracts of the aqueous layer. The organic phase was then dried over anhydrous magnesium sulfate, filtered and concentrated to a semi-solid residue. Recrystallization from acetone gave 2,3-dihydrospiro[naphthalene-1(4H),3'- piperidine]-2',4,6'-trione, melting point 197°-199°C.

Therapeutic Function

Sedative, Hypnotic

Check Digit Verification of cas no

The CAS Registry Mumber 2897-83-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2897-83:
(6*2)+(5*8)+(4*9)+(3*7)+(2*8)+(1*3)=128
128 % 10 = 8
So 2897-83-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H13NO3/c16-11-5-7-14(8-6-12(17)15-13(14)18)10-4-2-1-3-9(10)11/h1-4H,5-8H2,(H,15,17,18)

2897-83-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name spiro[2,3-dihydronaphthalene-4,3'-piperidine]-1,2',6'-trione

1.2 Other means of identification

Product number -
Other names 2,3-dihydrospiro[naphthalene-1(4H),3'-piperidine]-2',4,6'-trione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2897-83-8 SDS

2897-83-8Downstream Products

2897-83-8Relevant academic research and scientific papers

Methods of inducing sedation using certain spiroalkanone-imides

-

, (2008/06/13)

Compounds having the general formula: SPC1 Wherein R1 and R2 represent hydrogen, halogen, lower alkyl, lower alkoxy, or nitro, and wherein R1 and R2 may be the same or different. R3 may be hydrogen or lower alkyl, and X and Y may be one or two. They have been found to be useful sedative type depressants of the central nervous system. Most of the compounds having the general formula indicated above are new but others such as 2,3-dihydrospiro[naphthalene-1(4H),3'-piperidine]-2',4,6'-trione which has useful sedative properties have been reported in the literature.

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