647035-18-5 Usage
Molecular structure
The compound consists of an 1-octanol backbone linked to 3,7-dimethyl-8-(phenylmethoxy) and 4-methylbenzenesulfonate groups.
Stereochemistry
The (3R,7S)designation indicates the specific stereochemistry of the molecule, with the R configuration at the third carbon and the S configuration at the seventh carbon.
Physical properties
The physical properties of 1-Octanol, 3,7-dimethyl-8-(phenylmethoxy)-, 4-methylbenzenesulfonate,
(3R,7S)- are not explicitly provided in the material, but it is likely a liquid or solid based on its molecular structure.
Industrial applications
The compound may have various industrial applications, including use as a solvent, intermediate, or reagent in organic synthesis.
Safety considerations
It is important to handle 1-Octanol, 3,7-dimethyl-8-(phenylmethoxy)-, 4-methylbenzenesulfonate,
(3R,7S)- with care, as it may have hazardous properties. Specific safety considerations are not provided in the material.
Check Digit Verification of cas no
The CAS Registry Mumber 647035-18-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,7,0,3 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 647035-18:
(8*6)+(7*4)+(6*7)+(5*0)+(4*3)+(3*5)+(2*1)+(1*8)=155
155 % 10 = 5
So 647035-18-5 is a valid CAS Registry Number.
647035-18-5Relevant academic research and scientific papers
Enantioselective synthesis of three stereoisomers of 5,9- dimethylpentadecane, sex pheromone component of Leucoptera coffeella, from (-)-isopulegol
Moreira, Jardel A.,Correa, Arlene G.
, p. 3787 - 3795 (2007/10/03)
The coffee leaf miner, Leucoptera coffeella, is an economically important pest of coffee trees in Brazil. It has been demonstrated that the main sex pheromone component of this species is 5,9-dimethylpentadecane, however the stereochemistry of the natural
