101996-38-7 Usage
Chirality
Chiral compound
Enantiomeric forms
R and S
Active enantiomer
R form
Applications
a. Reagent in the synthesis of pharmaceuticals and agrochemicals
b. Building block in the production of other organic compounds
c. Intermediate in chemical synthesis
Pharmacological properties
a. Antioxidant activity
b. Anti-inflammatory activity
c. Antitumor activity
Structure
1,2-Benzenediol core with a 4-(2-amino-1-hydroxyethyl) substituent and a 5-chloro group
Stereochemistry
(R)configuration for the active enantiomer
Check Digit Verification of cas no
The CAS Registry Mumber 101996-38-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,9,9 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 101996-38:
(8*1)+(7*0)+(6*1)+(5*9)+(4*9)+(3*6)+(2*3)+(1*8)=127
127 % 10 = 7
So 101996-38-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H10ClNO3/c9-5-2-7(12)6(11)1-4(5)8(13)3-10/h1-2,8,11-13H,3,10H2/t8-/m0/s1
101996-38-7Relevant articles and documents
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.