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Benzoic acid, 2-[2-(4-morpholinyl)-1-cyclopenten-1-yl]-2-phenylhydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106689-99-0

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106689-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106689-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,6,8 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 106689-99:
(8*1)+(7*0)+(6*6)+(5*6)+(4*8)+(3*9)+(2*9)+(1*9)=160
160 % 10 = 0
So 106689-99-0 is a valid CAS Registry Number.

106689-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-(2-morpholinocyclopent-1-en-1-yl)-N'-phenylbenzohydrazide

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:106689-99-0 SDS

106689-99-0Relevant academic research and scientific papers

REACTIVITY OF CYCLOPENTANONE ENAMINES TOWARDS ACYL ARYLDIAZENES

Benedetti, Fabio,Forchiassin, Mirella,Russo, Claudio,Risaliti, Amerigo

, p. 663 - 668 (2007/10/02)

Reactions of 1-aminocyclopentenes 1 with acyl aryldiazenes 2 give 1:1 enaminic adducts 3 and 4, or 1,3,4-oxadiazines 5.Isolation of these products was not always possible in the reactions of 1-(piperidin-1-yl)- and 1-(pyrrolidin-1-yl)-cyclopentene.Acidic hydrolysis gave 2-(N-acyl-N'-aryl)hydrazinocyclopentanones 6 or 2-arylaminocyclopentenones 8, depending upon the amino moiety and the cyclic or open chain nature of the adducts.

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