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1,3-Dioxolane, 2,2-dimethyl-4-[(2-methylphenoxy)methyl]-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52094-00-5

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52094-00-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52094-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,9 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 52094-00:
(7*5)+(6*2)+(5*0)+(4*9)+(3*4)+(2*0)+(1*0)=95
95 % 10 = 5
So 52094-00-5 is a valid CAS Registry Number.

52094-00-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R)-2,2-dimethyl-4-[(2-methylphenoxy)methyl]-1,3-dioxolane

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:52094-00-5 SDS

52094-00-5Relevant academic research and scientific papers

Cardiovascular hybrid drugs: New benzazepinone derivatives as bradycardic agents endowed with selective β1-Non-competitive antagonism

Bisi, Alessandra,Rampa, Angela,Budriesi, Roberta,Gobbi, Silvia,Belluti, Federica,Ioan, Pierfranco,Valoti, Ermanno,Chiarini, Alberto,Valenti, Piero

, p. 1353 - 1361 (2007/10/03)

The synthesis and pharmacological profile of some hybrid compounds bearing both the benzazepinone moiety present in Zatebradine and typical β-blocker aryloxypropanolamine groups are described. The new compounds proved to be endowed with negative chronotropic and inotropic activity and are weak vasorelaxant agents. The cardiodepressant action is probably due to selective β1-noncompetitive reversible antagonism. Both enantiomers of the most active compound 5c were synthesized and they showed a different cardiovascular profile, that is (+)-(R)-enantiomer displays affinity for cardiac β1-adrenoceptors, while (-)-(S)-enantiomer shows specificity for vessel smooth muscle.

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