768345-73-9 Usage
Chemical structure
A benzene ring with two hydroxyl groups (1,2-benzenediol), a chloro group, an amino group, and a hydroxyethyl group attached to it.
Molecular weight
Approximately 172.6 g/mol
Functional groups
Hydroxyl (-OH), amino (-NH2), chloro (-Cl), and hydroxyethyl (-CH2CH2OH)
Stereochemistry
The presence of the (1S)-2-amino-1-hydroxyethyl group indicates a specific stereochemistry at the chiral center.
Derivative
A derivative of catechol, a type of polyphenol.
Pharmaceutical industry
Commonly used as a building block for the synthesis of various biologically active compounds.
Applications
Potential use in medicinal chemistry, herbal and dietary supplements, and drug development.
Therapeutic potential
Shown promise as an antioxidant, anti-inflammatory, and anti-cancer agent.
Research focus
An important area of research for its potential therapeutic uses and its unique structure.
Check Digit Verification of cas no
The CAS Registry Mumber 768345-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,8,3,4 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 768345-73:
(8*7)+(7*6)+(6*8)+(5*3)+(4*4)+(3*5)+(2*7)+(1*3)=209
209 % 10 = 9
So 768345-73-9 is a valid CAS Registry Number.
768345-73-9Relevant academic research and scientific papers
Comparative α- and β-adrenoceptor activity of 2- and 6-ring-chlorinated noradrenaline analogues
Squier,Van der Schyf,Oliver,Venter
, p. 457 - 460 (2007/10/02)
The α- and β-adrenoceptor activity of the 2- and 6-ring-chlorinated analogues of noradrenaline (norepinephrine) were evaluated in vitro. The 2-chloro-substituted analogue exhibits a far greater affinity for β1-chronotropic receptors than the 6-chloro-substituted analogue, whereas no significant differences are apparent for their α-adrenergic affinities.
