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5-amino-3-[2-(3,4-dimethoxyphenyl)ethyl]-1,2,3-oxadiazol-3-ium chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37744-08-4

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37744-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37744-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,4 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 37744-08:
(7*3)+(6*7)+(5*7)+(4*4)+(3*4)+(2*0)+(1*8)=134
134 % 10 = 4
So 37744-08-4 is a valid CAS Registry Number.

37744-08-4SDS

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 3-[2-(3,4-dimethoxyphenyl)ethyl]oxadiazol-3-ium-5-amine,chloride

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:37744-08-4 SDS

37744-08-4Relevant academic research and scientific papers

New NO-donors with antithrombotic and vasodilating activities, I: 3-arylalkyl-N-nitroso-5-sydnone imines

Rehse,Kampfe,Schleifer

, p. 483 - 487 (2007/10/02)

Nine nitrosimino title compounds were prepared. They inhibit the aggregation of human platelets induced by collagen with an IC50 = 0.7-33 μmol/L. The most active substance is the 3-phenylethyl derivtive 6b. The in vitro effect is mediated by an active metabolite which is formed by a photochemical reaction in the aggregometer. As the corresponding and so far unknown sydnone-5-cyanimines have no effect on platelets the metabolite is most certainly a NO-species. The activity of the sydnone-5-nitrimine 5b is in the same order of magnitude (IC50 = 7.5 μmol/L) as in the nitrosimines of type 6. The most active compound 6b was investigated for antithrombotic properties in a thrombosis model, where the thrombus formation was induced by a laser beam. 2 h after oral administration of 60 mg/kg of 6b to rats in venoles a 28% inhibition of thrombin formation was found. In arterioles this effect is more evident and a 48% inhibition is seen (the thrombus formation index is 2.6 and 3.9, respectively). These results suggest that the active metabolite is formed as well in vivo.

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