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128960-12-3

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128960-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128960-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,9,6 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 128960-12:
(8*1)+(7*2)+(6*8)+(5*9)+(4*6)+(3*0)+(2*1)+(1*2)=143
143 % 10 = 3
So 128960-12-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H30N2O3S/c1-4-7-13(8-5-2)15(18)16-14-9-11-17(12-10-14)21(19,20)6-3/h13-14H,4-12H2,1-3H3,(H,16,18)

128960-12-3SDS

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 N-(1-ethylsulfonylpiperidin-4-yl)-2-propylpentanamide

1.2 Other means of identification

Product number -
Other names -

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:128960-12-3 SDS

128960-12-3Downstream Products

128960-12-3Relevant articles and documents

POTENTIAL ANTICONVULSANTS: SOME DERIVATIVES AND ANALOGUES OF 2-PROPYLPENTANOIC ACID

Valenta, Vladimir,Vejdelek, Zdenek,Sindelar, Karel,Protiva, Miroslav

, p. 1067 - 1076 (2007/10/02)

Reaction of 2-(ethoxycarbonylamino)ethanol with 2-propylpentanoyl chloride gave the ester III.N-(4-Piperidinyl)-2-propylpentanamide (V) was prepared via the 1-benzyl-4-piperidinyl derivative IV and was acylated with ethanesulfonyl chloride and 2-propylpentanoyl chloride to give the amides VI and VII.Malonic ester syntheses afforded diethyl 2-ethyl- and 2-propyl-2-(2(methylthio)ethyl)malonate VIII and XIII which were hydrolyzed and decarboxylated to the acids X and XV which, in turn, were transformed to the amides XII and XVII. 3-Thiapentanenitrile was alkylated with propyl bromide to the nitrile XIX which was hydrolyzed to the acid XX and the amide XXI.The acids X, XV, and XX, and the amides XII, XVII, and XXI are analogues of the anticonvulsant agents valproic acid (I) and valpromide (II).Compounds XX (VFB-14 721) and XXI (VFB-14 722) potentiate, in doses in which they "per se" are ineffective as anticonvulsants in mice, significantly the anticonvulsant effect of diazepam.

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