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N-(5-methyl-1,3,4-oxadiazol-2-yl)acetamide is a chemical compound with the molecular formula C5H8N2O3. It is a derivative of acetamide, featuring a 5-methyl-1,3,4-oxadiazol-2-yl group attached to the nitrogen atom. This heterocyclic ring system provides the molecule with unique electronic and steric properties, which can influence its reactivity and potential applications. The compound is often used in organic synthesis as a building block for more complex molecules, particularly in pharmaceuticals and agrochemicals, due to its ability to act as a protecting group or a reactive intermediate. Its stability and reactivity make it a valuable tool in the synthesis of various biologically active compounds.

5378-58-5

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5378-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5378-58-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,7 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5378-58:
(6*5)+(5*3)+(4*7)+(3*8)+(2*5)+(1*8)=115
115 % 10 = 5
So 5378-58-5 is a valid CAS Registry Number.

5378-58-5SDS

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-(5-methyl-1,3,4-oxadiazol-2-yl)acetamide

1.2 Other means of identification

Product number -
Other names N-(Methyl-[1,3,4]oxadiazol-2-yl)-acetamid

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 -
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More Details:5378-58-5 SDS

5378-58-5Relevant academic research and scientific papers

NOVEL REARRANGEMENT OF 3-ACYL-5-ACYLAMINO-2,3-DIHYDRO-1,3,4-THIADIAZOLE 1-OXIDE INTO 1,3,4-OXADIAZOLES

Kubota, Seiju,Toyooka, Kouhei,Yamamoto, Naoya,Kasai, Takayuki,Shibuya, Masayuki

, p. 21 - 24 (2007/10/02)

Thermally, or in the presence of p-toluenesulfonic acid, 3-acyl-5-acylamino-2,3-dihydro-1,3,4-thiadiazole 1-oxides are transformed into 1,3,4-oxadiazoles, carbonyl compounds and sulfur.

Stereoselective S-Oxidation of 5-Substituted 4-Acetyl-Δ2-1,3,4-thiadiazolines: X-Ray Crystal Structure of 4-Acetyl-2-acetylamino-5-methyl-5-phenyl-Δ2-1,3,4-thiadiazoline 1-Oxide

Kubota, Seiju,Toyooka, Kouhei,Yamamoto, Naoya,Shibuya, Masayuki,Kido, Masaru

, p. 901 - 902 (2007/10/02)

N.m.r. spectroscopy and X-ray crystallography show that oxidation of 5-substituted 4-acetyl-2-acetylamino-Δ2-1,3,4-thiadiazolines with m-chloroperbenzoic acid gives the corresponding Δ2-1,3,4-thiadiazoline 1-oxides; the novel reactions of the product (2a) are also described.

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