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1041005-85-9

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1041005-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1041005-85-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,1,0,0 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1041005-85:
(9*1)+(8*0)+(7*4)+(6*1)+(5*0)+(4*0)+(3*5)+(2*8)+(1*5)=79
79 % 10 = 9
So 1041005-85-9 is a valid CAS Registry Number.

1041005-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-3-p-tolyl-1,2,4-oxadiazol-5-amine

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:1041005-85-9 SDS

1041005-85-9Downstream Products

1041005-85-9Relevant articles and documents

Convenient synthesis and biological profile of 5-amino-substituted 1,2,4-oxadiazole derivatives

Ispikoudi, Maria,Amvrazis, Michalis,Kontogiorgis, Christos,Koumbis, Alexandros E.,Litinas, Konstantinos E.,Hadjipavlou-Litina, Dimitra,Fylaktakidou, Konstantina C.

experimental part, p. 5635 - 5645 (2011/02/22)

We describe herein a convenient straightforward synthesis of 5-amino-substituted 1,2,4-oxadiazoles, upon the reactions of amidoximes with carbodiimides, as well as their further derivatization to acetamides, in good yields. Most of the compounds exhibited in general low interaction with the stable radical 1,1-diphenyl-2-picryl-hydrazyl. Compounds 32 and 39 inhibited significantly soybean lipoxygenase. Selected compounds were screened for their in vivo anti-inflammatory activity using the carrageenin paw edema model and showed significant anti-inflammatory activity (26, 51%). The ability of the compounds to release NO in the presence of a thiol factor has been also investigated.

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