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220120-58-1

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220120-58-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220120-58-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,1,2 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 220120-58:
(8*2)+(7*2)+(6*0)+(5*1)+(4*2)+(3*0)+(2*5)+(1*8)=61
61 % 10 = 1
So 220120-58-1 is a valid CAS Registry Number.

220120-58-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 8-METHYL-3,4-DIHYDRO-2H-1,4-BENZOXAZINE-2-CARBOXYLATE

1.2 Other means of identification

Product number -
Other names 2H-1,4-Benzoxazine-2-carboxylicacid,3,4-dihydro-8-methyl-,ethyl ester

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:220120-58-1 SDS

220120-58-1Downstream Products

220120-58-1Relevant articles and documents

Synthesis and biological evaluation of new 2-(4,5-dihydro-1H-imidazol-2-yl)-3,4-dihydro-2H-1,4-benzoxazine derivatives

Touzeau, Frédérique,Arrault, Axelle,Guillaumet, Gérald,Scalbert, Elizabeth,Pfeiffer, Bruno,Rettori, Marie-Claire,Renard, Pierre,Mérour, Jean-Yves

, p. 1962 - 1979 (2007/10/03)

2-(4,5-Dihydro-1H-imidazol-2-yl)-3,4-dihydro-2H-1,4-benzoxazine derivatives and tricyclic analogues with a fused additional ring on the nitrogen atom of the benzoxazine moiety have been prepared and evaluated for their cardiovascular effects as potential antihypertensive agents. The imidazoline ring was generated by reaction of the corresponding ethyl ester with ethylenediamine. Affinities for imidazoline binding sites (IBS) I1 and I2 and α1 and α2 adrenergic receptors were evaluated as well as the effects on mean arterial blood pressure (MAP) and heart rate (HR) of spontaneously hypertensive rats. With few exceptions the most active compounds on MAP were those with high affinities for IBS and α2 receptor. Among these, compound 4h was the most interesting and is now, together with its enantiomers, under complementary pharmacological evaluation.

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