1242272-80-5 Usage
Functional groups
Fluorine atom, aromatic ring, methylbutynyl group
Structural features
a. Fluorine atom attached to the first carbon of the benzene ring
b. Methylbutynyl group attached to the fourth carbon of the benzene ring
c. Methyl group on the butynyl chain
Aromatic compound
Yes
Fluorinated compound
Yes
Applications
a. Organic synthesis
b. Building block for complex organic molecules
c. Pharmaceutical industry
d. Agrochemical industry
e. Fine chemicals and materials production
f. Research and development in chemical and pharmaceutical industries
Physical state
Likely a liquid or solid at room temperature (based on molecular size and complexity)
Solubility
Likely soluble in organic solvents such as ethanol, acetone, or dichloromethane
Stability
Stable under normal conditions, but may be sensitive to heat, light, or strong acids/bases
Reactivity
May undergo reactions such as electrophilic aromatic substitution, nucleophilic substitution, and free radical reactions due to the presence of the aromatic ring and fluorine atom.
Check Digit Verification of cas no
The CAS Registry Mumber 1242272-80-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,2,2,7 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1242272-80:
(9*1)+(8*2)+(7*4)+(6*2)+(5*2)+(4*7)+(3*2)+(2*8)+(1*0)=125
125 % 10 = 5
So 1242272-80-5 is a valid CAS Registry Number.
1242272-80-5Relevant articles and documents
Dual Gold Catalysis: Synthesis of Fluorene Derivatives from Diynes
Bucher, Janina,Wurm, Thomas,Taschinski, Svenja,Sachs, Eleni,Ascough, David,Rudolph, Matthias,Rominger, Frank,Hashmi, A. Stephen K.
, p. 225 - 233 (2017/02/05)
1,5-Diyne systems bearing one terminal and one benzyl- or allyl-substituted alkyne attached to an aromatic backbone were converted in the presence of a gold catalyst. In a dual gold-catalyzed process, gold vinylidenes are formed that selectively undergo formal CH insertion into the C(sp2)–H bond of the offered unsaturated systems. If H atoms are present in the propargylic position, a subsequent isomerization to the aromatic system takes place leading to 9H-fluorene and 11H-benzo[b]fluorene derivatives as final products. In the case of a quaternary carbon in the propargylic position no further aromatization is observed and 10H-benzo[b]fluorene derivatives are obtained in high yield. (Figure presented.).
Novel homopropargylamines
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, (2008/06/13)
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