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1,4-Diazaspiro[4.5]decan-2-one, 3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16256-40-9

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16256-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16256-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,5 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16256-40:
(7*1)+(6*6)+(5*2)+(4*5)+(3*6)+(2*4)+(1*0)=99
99 % 10 = 9
So 16256-40-9 is a valid CAS Registry Number.

16256-40-9SDS

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 2-phenyl-1,4-diazaspiro[4.5]decan-3-one

1.2 Other means of identification

Product number -
Other names 2,2-pentamethylene-5-phenylimidazolidone-4

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:16256-40-9 SDS

16256-40-9Relevant academic research and scientific papers

IMIDAZOLINONE DERIVATIVES AS CGRP RECEPTOR ANTAGONISTS

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Page/Page column 82, (2010/08/04)

The present invention is directed to imidazolinone derivatives which are antagonists of CGRP receptors and useful in the treatment or prevention of diseases in which CGRP is involved, such as migraine. The invention is also directed to pharmaceutical comp

Glyt1 Transporter Inhibitors and Uses Thereof in Treatment of Neurological and Neuropsychiatric Disorders

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Page/Page column 28-29, (2008/12/08)

The invention provides a compound of formula (I) or a solvate thereof: wherein R1, R2, R3, R4, R5, R6, and n are as defined in the specification, and uses of such compounds. The compounds i

Zeolite-induced heterocyclization: A superior method of synthesis of imidazolidinones

Nooshabadi, Massoud A.,Aghapoor, Kioumars,Bolourtchian, Mohammad,Heravi, Majid M.

, p. 498 - 499 (2007/10/03)

A superior method for synthesis of imidazolidinones by catalytic action of H-Y zeolite from the reaction of α-aminocarboxamides with carbonyl compounds is described.

Synthesis of Novel Imidazolidinones

Khalaj,Bazaz,Shekarchi

, p. 395 - 398 (2007/10/03)

The preparation of a number of new imidazolidinones by a simple method based on the reaction of α-aminocarboxamides with carbonyl compounds is described.

Reactions of α-phenylglycinamide with some carbonyl compounds. Formation of 5,7-diisopropyl-8,8-dimethyl-2-oxo-3-phenylimidazolidino-tetrahydro--oxazine, and determination of structure and stereochemistry by nuclear Overhauser effect differenc

Qing, Ning,Colebrook, Lawrence D.,Edward, John T.,Kon, Allan,Chubb, Francis L.

, p. 1560 - 1564 (2007/10/02)

α-phenylglycinamide 5 reacts with ketones to give either the Schiff base 3 or the 4-imidazolidone 4, but reacts with boiling isobutyraldehyde to give the bicyclic compound 6.The structure and stereochemistry of 6 have been established by (1)H nuclear Over

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