5411-95-0 Usage
Chemical class
Belongs to the class of bisphenol compounds.
Common use
Used as a precursor in the synthesis of various pharmaceutical and agrochemical products.
Antimicrobial properties
Known for its ability to inhibit the growth of certain bacteria and fungi, making it an effective antimicrobial agent.
Industrial applications
Used in the production of epoxy resins and as a stabilizer in PVC plastics.
Toxicity
Considered toxic and may pose health risks if not used properly.
Chemical structure
The compound has a central ethanol molecule with two 4-chlorophenyl groups attached to the 1,2 positions and a (2-hydroxyethyl)amino group attached to the 2 position.
Check Digit Verification of cas no
The CAS Registry Mumber 5411-95-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5411-95:
(6*5)+(5*4)+(4*1)+(3*1)+(2*9)+(1*5)=80
80 % 10 = 0
So 5411-95-0 is a valid CAS Registry Number.
5411-95-0Relevant articles and documents
Substituted dialkanolamines, sulfur analogs and condensed 1,4-oxazine derivatives thereof in viral disease treatment
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, (2008/06/13)
Substituted dialkanolamines, oxazine and sulfur analogs thereof, useful in treating shipping fever syndrome in mammals are disclosed having the formula: STR1 wherein: Ar is STR2 Z is oxygen or sulfur; R is selected from hydrogen, loweralkyl or STR3 R1 R2, R3, R4, R5, R6 and R7 are selected from hydrogen or loweralkyl; and STR4 when taken together may form a lowercycloalkyl ring or R5 with --ZR2 when taken together may form a 5-membered saturated oxygen or sulfur containing heterocyclic ring; X is selected from hydrogen, halo, loweralkoxy, loweralkyl, trifluoromethyl or dimethylamino and when X is more than 1, it may be the same radical or different; y is 0, 1 or 2; n is one, or zero and when n is 1, the stereoisomers thereof and when n is zero the dotted line becomes an oxygen-carbon bond forming an oxazine ring and the pharmaceutically acceptable acid addition salts thereof.