246229-01-6 Usage
Description
2,5-Cyclohexadien-1-one,4-fluoro-3,4,5-trimethyl-(9CI) is a chemical compound with the molecular formula C10H13FO. It is a yellow, oily liquid with a strong, fruity odor.
Used in Pharmaceutical Industry:
2,5-Cyclohexadien-1-one,4-fluoro-3,4,5-trimethyl-(9CI) is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of various medications.
Used in Agrochemical Industry:
2,5-Cyclohexadien-1-one,4-fluoro-3,4,5-trimethyl-(9CI) is also used as an intermediate in the synthesis of agrochemicals, playing a role in the production of substances that help protect crops and enhance agricultural productivity.
Used in Food and Beverage Industry:
2,5-Cyclohexadien-1-one,4-fluoro-3,4,5-trimethyl-(9CI) is used as a flavor and fragrance agent in the food and beverage industry, adding distinctive tastes and scents to products.
Safety Measures:
It is important to handle this compound with care, as it may be harmful if swallowed, inhaled, or absorbed through the skin, and can cause irritation to the eyes, skin, and respiratory system. Therefore, proper safety measures should be taken when working with this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 246229-01-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,6,2,2 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 246229-01:
(8*2)+(7*4)+(6*6)+(5*2)+(4*2)+(3*9)+(2*0)+(1*1)=126
126 % 10 = 6
So 246229-01-6 is a valid CAS Registry Number.
246229-01-6Relevant articles and documents
Transformations of organic molecules with F-TEDA-BF4 in ionic liquid media
Pavlinac, Jasminka,Zupan, Marko,Stavber, Stojan
experimental part, p. 2394 - 2409 (2009/12/03)
The transformations of organic molecules with F-TEDA-BF4 (1) were investigated in the hydrophilic ionic liquid (IL) 1-butyl-3-methyl- imidazolium tetrafluoroborate ([bmim][BF4], 2) and the hydrophobic IL 1-butyl-3-methyl-imidazolium hexafluorophosphate ([bmim][PF6], 3). The range of substrates included alkyl substituted phenols 4a-c, 9, 13, 1,1-diphenylethene (15), alkyl aryl ketones 19-22, aldehydes 23-25 and methoxy-substituted benzene derivatives 26-30. The evaluation of the outcome of reactions performed in IL media in comparison to those of the corresponding reactions in conventional organic solvents revealed that the transformations in IL are less efficient and selective. The effect of the presence of a nucleophile (MeOH, H2O, MeCN) on the course of reaction was also studied.
Efficient synthesis of 4-fluorocyclohexa-2,5-dienone derivatives using n-fluoro-1,4-diazoniabicyclo[2.2.2]octane salt analogues
Stavber, Stojan,Jereb, Marjan,Zupan, Marko
, p. 1375 - 1378 (2007/10/03)
4-Fluorocyclohexa-2,5-dienone derivatives were obtained in high yield by reaction of para substituted phenols with 1-fluoro-4-chloromethyl-1,4- diazoniabicyclo[2.2.2]octane bis(tetra-fluoro-borate) (1a, Selectfluor(TM) F- TEDA-BF4) or its 4-hyd
