113682-53-4 Usage
Chemical class
Piperidine derivatives
Molecular weight
227.3 g/mol
Application
Insect repellent
Mechanism of action
Creates a barrier that masks the user's smell, making them unattractive to insects
Effective against
Mosquitoes, ticks, fleas, and flies
Usage
Commonly used in lotions, sprays, and wipes
Purpose
Protection against insect bites and diseases they can transmit
Reputation
Highly effective and versatile insect repellent
Global usage
Widely used around the world
Check Digit Verification of cas no
The CAS Registry Mumber 113682-53-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,6,8 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 113682-53:
(8*1)+(7*1)+(6*3)+(5*6)+(4*8)+(3*2)+(2*5)+(1*3)=114
114 % 10 = 4
So 113682-53-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H19NO3/c1-8(13)15-12-10(2,3)6-9(14)7-11(12,4)5/h6-7H2,1-5H3
113682-53-4Relevant articles and documents
Synthesis and properties of bicyclic aziridines, derivatives of triacetoneamine
Krinitskaya
, p. 527 - 531 (2007)
Bicyclic aziridines, derivatives of 2,2,6,6-tetramethyl-4-piperidone (triacetoneamine), are synthesized, which by acids treatment undergo the N-C(1) or N-C(2) bonds cleavage to form the corresponding pyrrolines, pyrrolidines, and piperidines.
Conformationally Restricted Spin Labelled Nucleotides: a Model Study of the Synthesis and Properties of the 2',3'-O-Spiro Ketal of Uridine and 4-oxo-2,2,6,6-tetramethyl-1-piperidyloxy
Alessi, Dario R.,Corrie, John E. T.,Feeney, James,Trayer, Ian P.,Trentham, David R.
, p. 2243 - 2247 (2007/10/02)
The synthesis of 2',3'-O-(1-oxy-2,2,6,6-tetramethyl-4-piperidylidene)uridine 13 is described in a model study directed at the corresponding spin labelled spiro ketal derivative of ATP (adenosine triphosphate) 1 and of other nucleotides.The synthesis proce