207604-99-7 Usage
Fluorinated derivative of pentalen-7-one
The compound is a modified version of pentalen-7-one, in which a fluorine atom is added to the molecule.
Organic compound class
ketones The compound belongs to the class of organic compounds known as ketones, which are characterized by the presence of a carbonyl group (C=O) bonded to two carbon atoms.
Colorless liquid
The compound is a colorless liquid, indicating that it does not have any color.
Boiling point
81-82°C The boiling point of the compound is the temperature at which it changes from a liquid to a gas. In this case, the compound boils at 81-82°C.
Building block and intermediate in the synthesis of pharmaceuticals and agrochemicals
The compound is used as a building block and intermediate in the synthesis of various pharmaceuticals and agrochemicals, due to its unique chemical structure and reactivity.
Flammability
The compound is flammable, meaning it can easily catch fire and burn.
Skin and eye irritant
The compound may cause irritation if it comes into contact with the skin or eyes, and should be handled with caution.
Check Digit Verification of cas no
The CAS Registry Mumber 207604-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,6,0 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 207604-99:
(8*2)+(7*0)+(6*7)+(5*6)+(4*0)+(3*4)+(2*9)+(1*9)=127
127 % 10 = 7
So 207604-99-7 is a valid CAS Registry Number.
207604-99-7Relevant academic research and scientific papers
Kaselj, Mira,Gonikberg, Elena M.,Le Noble, William J.
, p. 3218 - 3223 (1998)
The effects of 3-halo substitution on face selection in borohydride reductions of both nor- and homoadamantan-9-ones 1-X and 3-X, respectively, have been compared with those of 5-halo substitution in the parent 5-haloadamantan-2-ones 2-X. The differences between the product ratios in these three compounds are small, but the selectivity of 2-X is somewhat larger than that of either of the homologues. This is also true of the corresponding aza- and diazaadamantanones, and of an electrophilic addition. It is concluded that the approach angle of the reagent is not a sensitive variable in addition reactions of cyclohexanone and its derivatives, and that well-aligned antiperiplanar bonds are preferred to achieve maximal remote substituent induced selectivities.
