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Benzaldehyde, (5,5-dimethyl-1,3,4-oxadiazol-2(5H)-ylidene)hydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54871-23-7

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54871-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54871-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,7 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54871-23:
(7*5)+(6*4)+(5*8)+(4*7)+(3*1)+(2*2)+(1*3)=137
137 % 10 = 7
So 54871-23-7 is a valid CAS Registry Number.

54871-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name benzaldehyde (Ξ)-((Z)-5,5-dimethyl-5H-[1,3,4]oxadiazol-2-ylidene)-hydrazone

1.2 Other means of identification

Product number -
Other names N-[5,5-Dimethyl-5H-[1,3,4]oxadiazol-(2Z)-ylidene]-N'-[1-phenyl-meth-(Z)-ylidene]-hydrazine

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:54871-23-7 SDS

54871-23-7Downstream Products

54871-23-7Relevant academic research and scientific papers

Oxadiazoline derivatives

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, (2008/06/13)

Benzylidenehydrazono-oxadiazoline compounds have been prepared of the formula: STR1 wherein R1 and R2 are both lower alkyl or form with the heterocyclic ring carbon atom an alicyclic ring; and R3 when present is selected from halogen, lower alkyl and lower alkoxy. The preparation involves condensing a benzaldehyde with carbodihydrazide and further condensing with a ketone (or vice versa) to form the corresponding crossed carbodihydrazone, and oxidizing and cyclizing to form the oxadiazoline derivatives. These derivatives have analgesic and/or anti-inflammatory activity.

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