58851-63-1 Usage
Uses
Used in Pharmaceutical Industry:
a-Bromo-cyclohexaneacetic acid Methyl ester is used as a reagent for the preparation of various pharmaceuticals and research chemicals. Its unique chemical structure allows it to be a valuable component in the synthesis of new and existing drugs, contributing to the development of novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, a-Bromo-cyclohexaneacetic acid Methyl ester is utilized as an intermediate in the production of other organic compounds. Its versatile chemical properties make it a useful building block for the synthesis of a wide range of organic molecules, including complex organic structures and specialty chemicals.
Used in Medicinal Chemistry Research:
a-Bromo-cyclohexaneacetic acid Methyl ester is employed as a research chemical in medicinal chemistry, where it is used to study the structure-activity relationships of various drug candidates. Its unique functional groups and reactivity enable researchers to explore new chemical pathways and develop innovative therapeutic agents with improved efficacy and safety profiles.
Used in Laboratory Settings:
Due to its potentially hazardous nature, a-Bromo-cyclohexaneacetic acid Methyl ester is commonly handled and synthesized in laboratory settings. Strict safety protocols are followed to ensure the safe handling, storage, and disposal of this chemical compound, minimizing the risk of accidents and exposure to laboratory personnel.
Check Digit Verification of cas no
The CAS Registry Mumber 58851-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,5 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58851-63:
(7*5)+(6*8)+(5*8)+(4*5)+(3*1)+(2*6)+(1*3)=161
161 % 10 = 1
So 58851-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H15BrO2/c1-12-9(11)8(10)7-5-3-2-4-6-7/h7-8H,2-6H2,1H3
58851-63-1Relevant academic research and scientific papers
Privileged structure based ligands for melanocortin-4 receptors-Aliphatic piperazine derivatives
Briner, Karin,Collado, Iván,Fisher, Matthew J.,García-Paredes, Cristina,Husain, Saba,Kuklish, Steven L.,Mateo, Ana I.,O'Brien, Thomas P.,Ornstein, Paul L.,Zgombick, John,de Frutos, óscar
, p. 3449 - 3453 (2007/10/03)
Aliphatic carbocyclic replacement of the benzyl group of compound 1 yielded compounds with high affinity for the melanocortin-4 receptor (MC4R). Compounds with a cyclohexyl group showed a consistent high affinity, while different polar groups with less basicity were good replacements for the original diethyl amines. Substitution of the polar group found in these privileged structures with an aliphatic moiety produced compounds with high affinity for MC4R.
