230295-09-7 Usage
General Description
2,3,6-TRIFLUOROBENZYLAMINE is a chemical compound with the molecular formula C7H6F3N. It is a derivative of benzylamine, with fluorine atoms substituted at the 2, 3, and 6 positions of the benzene ring. 2,3,6-TRIFLUOROBENZYLAMINE is commonly used in organic synthesis as a building block for the preparation of various pharmaceuticals, agrochemicals, and other specialty chemicals. It has applications in the manufacturing of anti-fungal agents, insecticides, and pharmaceuticals. 2,3,6-TRIFLUOROBENZYLAMINE is also used as a reagent in organic chemistry for various transformations, such as in the formation of carbon-carbon and carbon-nitrogen bonds. Additionally, it is utilized as a starting material in the production of dyes, pigments, and polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 230295-09-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,0,2,9 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 230295-09:
(8*2)+(7*3)+(6*0)+(5*2)+(4*9)+(3*5)+(2*0)+(1*9)=107
107 % 10 = 7
So 230295-09-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H6F3N/c8-5-1-2-6(9)7(10)4(5)3-11/h1-2H,3,11H2
230295-09-7Relevant articles and documents
The pattern of fluorine substitution affects binding affinity in a small library of fluoroaromatic inhibitors for carbonic anhydrase
Doyon, Jeffrey B.,Jain, Ahamindra
, p. 183 - 185 (1999)
(equation presented) A library of fluoroaromatic inhibitors of carbonic anhydrase has been found to bind in a manner dependent on both hydrophobicity and the pattern of substitution of the fluoroaromatic ring. All of the compounds in the library bind to the protein with Kd 3 nM. We have inferred two distinct binding modes from our data, which suggest two types of interactions that should be considered when designing fluorinated drugs.
