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6-phenyl-1,3-diazaspiro[4.5]decane-2,4-dione is a complex organic compound with a unique molecular structure. It is characterized by a spiro ring system, which consists of two fused rings sharing a common atom. In this case, the spiro ring system is composed of a 1,3-diazaspiro[4.5]decane and a phenyl group. The compound also features two carbonyl groups (dione) at the 2 and 4 positions, which contribute to its reactivity and potential applications. This chemical is primarily of interest to researchers in the fields of organic chemistry and medicinal chemistry, as its structure may possess specific biological activities or serve as a building block for the synthesis of more complex molecules.

5007-36-3

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5007-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5007-36-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5007-36:
(6*5)+(5*0)+(4*0)+(3*7)+(2*3)+(1*6)=63
63 % 10 = 3
So 5007-36-3 is a valid CAS Registry Number.

5007-36-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-phenyl-1,3-diazaspiro[4.5]decane-2,4-dione

1.2 Other means of identification

Product number -
Other names 10-phenyl-2,4-diazaspiro[4.5]decane-1,3-dione

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:5007-36-3 SDS

5007-36-3Relevant academic research and scientific papers

New spirohydantoin derivatives - Synthesis, pharmacological evaluation, and molecular modeling study

Czopek, Anna,Zagórska, Agnieszka,Ko?aczkowski, Marcin,Bucki, Adam,Gryz?o, Beata,Rychtyk, Joanna,Paw?owski, Maciej,Siwek, Agata,Sata?a, Grzegorz,Bojarski, Andrzej,Kubacka, Monika,Filipek, Barbara

, p. 1545 - 1554 (2016/12/18)

A series of new arylpiperazinylpropyl derivatives of 8/6-phenyl-1,3-diazaspiro[4.5]decan-2,4-dione and spiro[imidazolidine-4,1′-indene/naphthalene]-2,5-dione was synthesized and their affinity was evaluated toward serotonin 5-HT1A, 5-HT2A

Novel spirohydantoin derivative as a potent multireceptor-active antipsychotic and antidepressant agent

Czopek, Anna,Ko?aczkowski, Marcin,Bucki, Adam,Byrtus, Hanna,Paw?owski, Maciej,Kazek, Grzegorz,Bojarski, Andrzej J.,Piaskowska, Agata,Kalinowska-T?ücik, Justyna,Partyka, Anna,Weso?owska, Anna

, p. 3436 - 3447 (2015/08/03)

Abstract A series of novel spirohydantoin derivatives with arylpiperazinylbutyl moiety were synthesized and evaluated for serotonin 5-HT1A, 5-HT2A, 5-HT7 and dopamine D2 receptors. Based on these data, four comp

Stereochemistry of the conventional and modified Bucherer-Bergs reactions of 2-substituted cyclohexanones

Sacripante, Guerino,Edward, John T.

, p. 1982 - 1987 (2007/10/02)

The configurations of the spiro-hydantoins produced from 2-methyl- and 2-phenylcyclohexanone, 2,6-dimethylcyclohexanone, and dl-menthone by either the conventional Bucherer-Bergs (B.-B.) reaction, or a variant employing COS or CS2 in place of C

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