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3-(hydroxymethyl)-1,3-diazaspiro[4.5]decane-2,4-dione is a complex organic compound with the molecular formula C7H12N2O3. It features a spiro ring system, which consists of a seven-membered azaspiro ring fused to a five-membered diazane ring. The compound has two carbonyl groups at positions 2 and 4, and a hydroxymethyl group at position 3. This unique structure endows it with potential applications in various fields, such as pharmaceuticals and chemical research. Due to its specific functional groups and ring system, it may exhibit interesting chemical properties and reactivity, making it a subject of interest for further investigation and potential development.

710-86-1

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710-86-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 710-86-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 710-86:
(5*7)+(4*1)+(3*0)+(2*8)+(1*6)=61
61 % 10 = 1
So 710-86-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H14N2O3/c12-6-11-7(13)9(10-8(11)14)4-2-1-3-5-9/h12H,1-6H2,(H,10,14)

710-86-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(hydroxymethyl)-1,3-diazaspiro[4.5]decane-2,4-dione

1.2 Other means of identification

Product number -
Other names 3-hydroxymethyl-1,3-diaza-spiro[4.5]decane-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:710-86-1 SDS

710-86-1Downstream Products

710-86-1Relevant academic research and scientific papers

Spiromustine analogues. Relationships between structure, plasma stability, and antitumor activity

Haces,Driscoll,Roth,Heideman,Kelley

, p. 313 - 316 (1986)

Spiromustine is a hydantoin-containing nitrogen mustard currently in Phase I clinical trial. Since the in vitro plasma half-life of this compound (6.4 min, 37°C, pH 7.4) appeared to be influenced by the hydantoin ring, analogues containing 2-5 methylene spacer groups between this ring and the nitrogen mustard moiety were prepared and evaluated for hydrolytic stability and antitumor activity. Stability correlated with structure and pK(a) values. The proximity of the hydantoin ring to the mustard function was a stabilizing factor. Activity against murine P-388 leukemia was demonstrated and a gradual decrease in this activity was observed as the hydrolytic instability increased. A relationship between analogue structure and a mass spectral rearrangement ion was identified.

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