398136-39-5 Usage
Physical State
White to light brown solid at room temperature
Solubility
Soluble in alcohol and ether
Application
Intermediate in the production of various chemicals
Used in the synthesis of dyestuffs and pharmaceuticals
Primary Use
Pharmaceutical industry as a precursor in drug synthesis
Synthesis of antifungal and antibacterial agents
Additional Properties
Studied for potential antioxidant and anti-inflammatory properties
Considered in the development of new pharmaceutical products
Check Digit Verification of cas no
The CAS Registry Mumber 398136-39-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,8,1,3 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 398136-39:
(8*3)+(7*9)+(6*8)+(5*1)+(4*3)+(3*6)+(2*3)+(1*9)=185
185 % 10 = 5
So 398136-39-5 is a valid CAS Registry Number.
398136-39-5Relevant articles and documents
Chiral relay effect: 4-substituted 1,3-benzoxazol-2-(3H)-ones as achiral templates for enantioselective Diels-Alder reactions
Quaranta, Laura,Corminboeuf, Olivier,Renaud, Philippe
, p. 39 - 41 (2007/10/03)
(matrix presented) A new strategy to control the enantioselectivity of Lewis acid catalyzed reactions has been investigated. The use of N-acryloyl-1,3-benzoxazol-2-(3H)-ones substituted at position 4 leads to the formation of diastereomeric complexes as a
