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132382-13-9

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132382-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132382-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,8 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 132382-13:
(8*1)+(7*3)+(6*2)+(5*3)+(4*8)+(3*2)+(2*1)+(1*3)=99
99 % 10 = 9
So 132382-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H21N2O3.HI/c1-13(2,3)7-8-16-11(15)9-12-6-4-5-10(12)14;/h4-9H2,1-3H3;1H/q+1;/p-1

132382-13-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-[2-[2-(2-oxopyrrolidin-1-yl)acetyl]oxyethyl]azanium,iodide

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:132382-13-9 SDS

132382-13-9Downstream Products

132382-13-9Relevant articles and documents

POTENTIAL NOOTROPIC AGENTS: SYNTHESIS OF SOME (2-OXO-1-PYRROLIDINYL)ACETAMIDES AND SOME RELATED COMPOUNDS

Valenta, Vladimir,Holubek, Jiri,Svatek, Emil,Valchar, Martin,Krejci, Ivan,Protiva, Miroslav

, p. 2756 - 2764 (2007/10/02)

Ethyl (2-oxo-1-pyrrolidinyl)acetate was transformed by ester exchange to the 2-dimethylaminoethyl ester VI which was converted to the choline iodide ester VII.The mixed anhydride of (2-oxo-1-pyrrolidinyl)acetic acid and monoethyl carbonate was reacted with ethyl aminoacetate to give the ester VIII which was transformed on the one hand to the amide IX, and to the 2-dimethylaminoethyl ester X on the other.Reaction of the latter with methyl iodide afforded a further choline iodide ester XI.Reactions of (2-oxo-1-pyrrolidinyl)acetyl chloride with 4-chloroaniline and 3-aminopyridine gave the amides XII and XIV.The anilide XIII was obtained from 2-(2-oxo-1-pyrrolidinyl)butyric acid and 4-chloroaniline by means of dicyclohexylcarbodiimide.The benzo analogue (XV) of piracetam (I) was synthesized from oxindole via the ester XVI.The anilide XII (VUFB-16 536) was found to potentiate significantly the anticonvulsant effect of diazepam in mice, to prolong the survival time of mice under conditions of nitrogen anoxia, and to prolong significantly the duration of the "gasping reflex" in mice.

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