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120425-64-1

120425-64-1

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120425-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120425-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,4,2 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 120425-64:
(8*1)+(7*2)+(6*0)+(5*4)+(4*2)+(3*5)+(2*6)+(1*4)=81
81 % 10 = 1
So 120425-64-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H21NO2/c1-3-6-10(7-4-2)12(15)13-9-5-8-11(13)14/h10H,3-9H2,1-2H3

120425-64-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-propylpentanoyl)pyrrolidin-2-one

1.2 Other means of identification

Product number -
Other names Vlp-pyd

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:120425-64-1 SDS

120425-64-1Downstream Products

120425-64-1Relevant articles and documents

SYNTHESIS AND NEUROTROPIC ACTIVITY OF A NUMBER OF N-LACTAMS

Ostrovskaya, R. U.,Trofimov, S. S.,Burov, Yu. V.,Likhosherstov, A. M.,Kovalev, G. I.,et al.

, p. 546 - 550 (1993)

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Synthesis of GABA-valproic acid derivatives and evaluation of their anticonvulsant and antioxidant activity

Rekatas, George V.,Tani, Ekaterini,Demopoulos, Vassilis J.,Kourounakis, Panos N.

, p. 393 - 398 (2007/10/03)

The synthesis and the anticonvulsant activity of a number of GABA and valproic acid derivatives are reported. The lipophilicity of these compunds and their inhibitory effect on lipid peroxidation were also investigated, in an effort to correlate the anticonvulsant activity with lipophilicity and inhibitory effect on lipid peroxidation. The synthetized compounds exhibited anticonvulsant effects which were stronger for the more lipophilic derivatives. One of the active anticonvulsants showed appreciable antioxidant properties. Finally, a good correlation was found between the experimentally derived (R(M)) and calculated (Σf and log P(SK)) lipophilicity for this series of compounds.

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