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3-AMINO-1,3-DIAZASPIRO[4.4]NONANE-2,4-DIONE is a bicyclic chemical compound derived from spiro nonane, featuring a diazaspiro backbone and an amino group. This unique structure consists of a five-membered and a seven-membered ring connected by a nitrogen bridge, along with two carbonyl groups. The presence of the amino group endows it with basic properties, allowing it to form salts with acids. Its distinctive spirocyclic framework and potential biological activity make it a promising candidate for applications in medicinal chemistry and drug design.

16252-62-3

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16252-62-3 Usage

Uses

Used in Medicinal Chemistry:
3-AMINO-1,3-DIAZASPIRO[4.4]NONANE-2,4-DIONE is used as a building block for the development of novel pharmaceutical compounds due to its unique spirocyclic structure and potential for biological activity.
Used in Drug Design:
In the pharmaceutical industry, 3-AMINO-1,3-DIAZASPIRO[4.4]NONANE-2,4-DIONE is utilized as a key intermediate in the synthesis of new drugs, leveraging its chemical properties to create molecules with specific therapeutic effects.

Check Digit Verification of cas no

The CAS Registry Mumber 16252-62-3 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 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16252-62:
(7*1)+(6*6)+(5*2)+(4*5)+(3*2)+(2*6)+(1*2)=93
93 % 10 = 3
So 16252-62-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H11N3O2/c8-10-5(11)7(9-6(10)12)3-1-2-4-7/h1-4,8H2,(H,9,12)

16252-62-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-AMINO-1,3-DIAZASPIRO[4.4]NONANE-2,4-DIONE

1.2 Other means of identification

Product number -
Other names 3-amino-1,3-diaza-spiro[4.4]nonane-2,4-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:16252-62-3 SDS

16252-62-3Downstream Products

16252-62-3Relevant academic research and scientific papers

Aminoderivatives of cycloalkanespirohydantoins: Synthesis and biological activity

Naydenova, Emilia,Pencheva, Nevena,Popova, Julita,Stoyanov, Neyko,Lazarova, Maria,Aleksiev, Boris

, p. 189 - 194 (2007/10/03)

3-Aminocycloalkanespiro-5-hydantoins were synthesized and their biological activity was studied. In contrast to hydantoins, these compounds failed to induce either anticonvulsive effects in the central nervous system or inhibitory effects on cholinergic contractions in the enteric nervous system. However, they exerted well pronounced, atropinsensitive, contractile effects on the guinea-pig ileum longitudinal muscle preparations. Structure-activity relationships established allow the assumption that: (i) the reduction of the ring size in the molecule of the spirohydantoins leads to an increase in the potency of the respective analogue to induce contractile effect; (ii) the introduction of -NH2 in position 3 increases the ability of all the compounds studied to exert contractions; (iii) the enlargement of the ring leads to: (1) an increase of the degree of desensitization of the preparations; and (2) a decrease (except 1a) of the potency of the analogues to exert contractile effects.

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