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39124-15-7

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39124-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39124-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,2 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 39124-15:
(7*3)+(6*9)+(5*1)+(4*2)+(3*4)+(2*1)+(1*5)=107
107 % 10 = 7
So 39124-15-7 is a valid CAS Registry Number.

39124-15-7SDS

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 8-Thia-1,3-diazaspiro[4.5]decane-2,4-dione

1.2 Other means of identification

Product number -
Other names 2,4-Diaza-8-thiaspiro[4.5]decan-1,3-dion

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:39124-15-7 SDS

39124-15-7Relevant articles and documents

Synthesis, DFT calculations and characterisation of new mixed Pt(II) complexes with 3-thiolanespiro-5'-hydantoin and 4-thio-1H-tetrahydropyranspiro-5'-hydantoin

Bakalova, Adriana,Nikolova-Mladenova, Boryana,Buyukliev, Rossen,Cherneva, Emiliya,Momekov, Georgi,Ivanov, Darvin

, p. 93 - 100 (2015/11/17)

Cisplatin is an anticancer drug widely used in the treatment of a wide range of solid tumours (head and neck, lung, bladder etc.), testicular and ovarian cancers. Because of its severe toxicity profile and spontaneous development of drug resistance in tumours, a number of Pt(II) complexes have been synthesised and tested for anti-tumour activity. Some of the investigations have focused on using ligands bearing donor atoms other than N (e.g., S, P, O). Two new mixed Pt(II) complexes of the general formula cis-[Pt(NH3)LCl2] where L is 3-thiolanespiro-5'-hydantoin and 4-thio-1H-tetrahydropyranspiro-5'-hydantoin were synthesised. The complexes were studied by elemental analysis, melting points, IR and 1H NMR spectra. The hybrid DFT calculations were used for optimisation of the structure geometries of the ligands III, IV and their Pt(II) complexes V and VI. The structural parameters so calculated, such as bond lengths and angles, are in good agreement with the experimental data for similar hydantoins and their platinum complexes. The results showed that the geometries of complexes V and VI are plane square and the bounding of ligands III and IV with platinum ions is effected by the sulphur atom from the cyclic ring. The complexes thus obtained were chemically examined in comparison with previously synthesised and published complexes of the general formula cis-[PtL2Cl2] (VII and VIII ) with the same ligands. The new compounds V and VI, as well as the previously investigated complexes (VII and VIII ), were analysed for cytotoxicity in vitro on SKW-3 and HL-60 human tumour cell lines. The results showed that all the complexes exerted concentration-dependent anti-proliferative activity.

A new series of cyclic amino acids as inhibitors of S-adenosyl L- methionine synthetase

Lavrador, Karine,Guillerm, Danielle,Guillerm, Georges

, p. 1629 - 1634 (2007/10/03)

Optically active 3-amino-3-(tetrahydrofuranyl) carboxylic acid, 3- amino-3-(tetrahydrothienyl) carboxylic acid and their corresponding six membered ring analogues have been synthesised and examined as potential inhibitors of the enzyme S-adenosylmethionine (AdoMet) synthetase. The kinetic behaviour of these compounds was studied using recombinant rat liver AdoMet synthetase (α-isoform) fractionated from E. coli transformed with the plasmid pSSRL-T7N. All the compounds tested were competitive inhibitors of the enzyme with respect to L-methionine.

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