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4-methyl-1,2,5-oxadiazole-3-carboxylic acid 2-oxide is a chemical compound with the molecular formula C5H5N2O4. It is a derivative of 1,2,5-oxadiazole, a five-membered heterocyclic ring containing two nitrogen atoms and one oxygen atom. The compound features a methyl group attached to the 4-position of the oxadiazole ring and a carboxylic acid group at the 3-position. The 2-oxide functional group indicates the presence of an oxygen atom double-bonded to the 2-position of the ring, which can influence the compound's reactivity and stability. This chemical is primarily used as a synthetic intermediate in the preparation of various pharmaceuticals and agrochemicals, owing to its unique structure and properties.

37132-22-2

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37132-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37132-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,1,3 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 37132-22:
(7*3)+(6*7)+(5*1)+(4*3)+(3*2)+(2*2)+(1*2)=92
92 % 10 = 2
So 37132-22-2 is a valid CAS Registry Number.

37132-22-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-2-oxido-1,2,5-oxadiazol-2-ium-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-methyl-2-oxy-furazan-3-carboxylic acid

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:37132-22-2 SDS

37132-22-2Relevant academic research and scientific papers

Pharmacochemistry of the furoxan ring: Recent developments

Calvino,Di Stilo,Fruttero,Gasco,Sorba,Gasco

, p. 321 - 334 (2007/10/02)

In the present work recent results obtained in the pharmacochemistry of the furoxan system are reported. In particular, after a brief description of the salient points of the furoxan chemistry, the synthesis and the properties of a series of Nifedipine and Prazosin analogues, containing this heterocyclic system, are described. Since we observed that a few furoxan derivatives are able to elicit both a dose-dependent rise in platelet cGMP levels and to promote a dose-dependent inhibition of AA-induced [Ca++] rise, and that many substituted furoxans show potent vasodilating and antiaggregatory activity, the possibility of using the furoxan system as a lead in the design of new vasodilators is also discussed.

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