76350-77-1 Usage
Explanation
The compound is named based on its structure, which consists of two benzene rings (biphenyl) with a fluoro group at the 2 position and a methyl group at the 3' position.
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), and fluorine (F) atoms in the molecule.
Explanation
The core structure of the compound is formed by two benzene rings connected by a single bond between their respective carbon atoms.
Explanation
A fluoro group (F) is attached to the second carbon atom of the biphenyl structure, which can influence the compound's properties.
Explanation
A methyl group (-CH3) is attached to the third carbon atom of the second benzene ring (3' position), further modifying the compound's properties.
Explanation
The presence of fluoro and methyl groups can affect the compound's solubility, boiling point, melting point, and other physical properties.
Explanation
The fluoro and methyl groups can impact the compound's reactivity, including its ability to form chemical bonds and undergo reactions.
Explanation
The presence of fluoro and methyl groups may influence the compound's interaction with biological systems, which could be relevant for pharmaceutical or agrochemical applications.
Explanation
The compound may have potential applications in various industries and research fields, but its specific uses and potential hazards should be further explored.
Explanation
The safety profile and potential hazards of the compound are not well-established and should be investigated to ensure proper handling and use.
Structure
Two benzene rings linked by a single carbon-carbon bond
Fluoro group
Present at the 2 position
Methyl group
Present at the 3' position
Physical Properties
Altered due to fluoro and methyl substitutions
Chemical Properties
Influenced by fluoro and methyl substitutions
Biological Activity
Potentially affected by fluoro and methyl substitutions
Industrial and Research Applications
Possible uses, but further investigation needed
Safety and Hazards
Unknown, requires further investigation
Check Digit Verification of cas no
The CAS Registry Mumber 76350-77-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,5 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76350-77:
(7*7)+(6*6)+(5*3)+(4*5)+(3*0)+(2*7)+(1*7)=141
141 % 10 = 1
So 76350-77-1 is a valid CAS Registry Number.
76350-77-1Relevant articles and documents
New synthesis of biaryls via Rh-catalyzed decarbonylative Suzuki-coupling of carboxylic anhydrides with arylboroxines
Goossen,Paetzold
, p. 1665 - 1668 (2004)
The catalytic cross-coupling of aromatic carboxylic anhydrides or acid chlorides with triarylboroxines has been achieved for the first time under decarbonylation, giving rise to the unsymmetrical biaryls rather than the expected diaryl ketones. This new decarbonylative Suzuki coupling, catalyzed by a [Rh(ethylene)2Cl]2/KF system, can be applied to aromatic, heteroaromatic and vinylic carboxylic anhydrides, potentially opening up new perspectives for the use of carboxylic acid derivatives as substrates in biaryl syntheses.
