5385-96-6 Usage
Molecular weight
208.22 g/mol
Class
Ester
Parent compounds
5-hydroxy-1-naphthalenecarboxylic acid and ethyl alcohol
Formation
Result of the reaction between an alcohol (ethyl alcohol) and a carboxylic acid (5-hydroxy-1-naphthalenecarboxylic acid)
Usage
Fragrance ingredient in perfumes and personal care products due to its pleasant odor
Biological activities
Potential antioxidant and anti-inflammatory properties
Versatility
Various potential applications in the fields of chemistry and biology
Check Digit Verification of cas no
The CAS Registry Mumber 5385-96-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,8 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5385-96:
(6*5)+(5*3)+(4*8)+(3*5)+(2*9)+(1*6)=116
116 % 10 = 6
So 5385-96-6 is a valid CAS Registry Number.
5385-96-6Relevant academic research and scientific papers
AMINOALCOHOL DERIVATIVES
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, (2008/06/13)
The present invention relates to a compound formula [I]: wherein Y is bond,--O--(CH2)n--(in which n is 1, 2, 3 or 4), etc., Z is cyano, tetrazolyl, etc., R1 is hydrogen, lower alkyl, etc., R2 is hydrogen or an amino protective group, R3 is hydrogen or lower alkyl, R4 is hydrogen or lower alkyl, R5 and R8 are each independently hydrogen, halogen, hydroxy, lower alkyl, etc., R6 is hydrogen, lower alkyl, etc., R9 is hydrogen or lower alkyl, and i is 1 or 2, or a salt thereof. The compound [I] of the present invention and pharmaceutically acceptable salts thereof are useful for the prophylactic and/or the therapeutic treatment of pollakiurea or urinary incontinence.
