55106-53-1 Usage
Chemical structure
1-Bromocyclohexanecarboxylic acid is an organic compound that contains a cyclohexane ring with a carboxylic acid group and a bromine substituent.
Functional groups
The compound has two main functional groups a carboxylic acid group and a bromine atom.
Reactivity
The bromine atom provides the compound with reactivity and can be used as a leaving group in substitution reactions.
Carboxylic acid group
The carboxylic acid group also provides reactivity, as it can undergo reactions such as esterification and amidation.
Applications
1-Bromocyclohexanecarboxylic acid is used in the synthesis of various organic compounds and pharmaceuticals.
Versatility
The compound is versatile with applications in organic synthesis and drug development.
Physical properties
The specific physical properties of 1-bromocyclohexanecarboxylic acid, such as melting point, boiling point, and solubility, are not provided in the material.
Chemical properties
The specific chemical properties of 1-bromocyclohexanecarboxylic acid, such as its reactivity with other compounds and its stability under different conditions, are not provided in the material.
Check Digit Verification of cas no
The CAS Registry Mumber 55106-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,0 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 55106-53:
(7*5)+(6*5)+(5*1)+(4*0)+(3*6)+(2*5)+(1*3)=101
101 % 10 = 1
So 55106-53-1 is a valid CAS Registry Number.
55106-53-1Relevant articles and documents
Cobalt-Catalyzed 1,4-Aryl Migration/Desulfonylation Cascade: Synthesis of α-Aryl Amides
Gillaizeau-Simonian, Nicolas,Barde, Etienne,Guérinot, Amandine,Cossy, Janine
, p. 4004 - 4008 (2021/02/11)
A cobalt-catalyzed 1,4-aryl migration/disulfonylation cascade applied to α-bromo N-sulfonyl amides was developed. The reaction was highly chemoselective, allowing the preparation of α-aryl amides possessing a variety of functional groups. The method was used as the key step to synthesize an alkaloid, (±)-deoxyeseroline. Mechanistic investigations suggest a radical process.
One-step conversion of ketones to conjugated acids using bromoform
Vitnik,Ivanovic,Vitnik,Orevic,Zizak,Juranic,Juranic
body text, p. 1457 - 1471 (2009/09/26)
Phase-transfer-catalyzed (PTC) reactions of ketones with bromoform and aqueous lithium hydroxide in alcoholic solvent result in the formation of ,-unsaturated carboxylic acids. The reaction was performed at room temperature for 24h. The corresponding conj
Homolytic aromatic substitution: A radical approach towards the synthesis of 5-azaoxindoles
Storey, John M.D.,Ladwa, Mitesh M.
, p. 381 - 383 (2007/10/03)
A range of 5-azaoxindoles have been synthesised employing homolytic aromatic substitution onto pyridine as the pivotal step.
