58096-29-0 Usage
Description
[1R-(1alpha,2beta,3alpha,5alpha)]-2,6,6-trimethylbicyclo[3.1.1]heptane-3-carboxylic acid is a bicyclic organic compound characterized by its carboxylic acid functional group and a rigid, stable three-dimensional structure. [1R-(1alpha,2beta,3alpha,5alpha)]-2,6,6-trimethylbicyclo[3.1.1]heptane-3-carboxylic acid's unique stereochemistry, denoted by the [1R-(1alpha,2beta,3alpha,5alpha)] designation, contributes to its potential applications in various fields, including organic synthesis, pharmaceuticals, and materials science.
Uses
Used in Organic Synthesis:
[1R-(1alpha,2beta,3alpha,5alpha)]-2,6,6-trimethylbicyclo[3.1.1]heptane-3-carboxylic acid is used as a key intermediate for the synthesis of various complex organic molecules. Its unique structure and functional group enable the creation of a wide range of compounds with diverse properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [1R-(1alpha,2beta,3alpha,5alpha)]-2,6,6-trimethylbicyclo[3.1.1]heptane-3-carboxylic acid is used as a building block for the development of new drugs. Its specific stereochemistry and functional group can be exploited to design molecules with targeted biological activities, potentially leading to the discovery of novel therapeutic agents.
Used in Materials Science:
[1R-(1alpha,2beta,3alpha,5alpha)]-2,6,6-trimethylbicyclo[3.1.1]heptane-3-carboxylic acid is utilized in the development of advanced materials with specific properties. Its unique structure and functional group can be incorporated into polymers, coatings, and other materials to enhance their performance characteristics, such as strength, durability, and chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 58096-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,9 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58096-29:
(7*5)+(6*8)+(5*0)+(4*9)+(3*6)+(2*2)+(1*9)=150
150 % 10 = 0
So 58096-29-0 is a valid CAS Registry Number.
58096-29-0Relevant articles and documents
Optically active transition-metal complexes, 8. - Transition-metal complexes of the optically active cyclopentadienyl ligand PinCp: Crystal structure of (S(Re))-(η5-PinCp)Re(No)(PPh3)[CONHCH(CH3)C10H7
Salzer, Albrecht,Hosang, Annegret,Knuppertz, Jutta,Englert, Ulli
, p. 1497 - 1505 (1999)
The synthesis of (η5-PinCp*)Re(CO)3 [PinCp* = tetramethyl(pinanyl)cyclopentadienyl] is described. Successive substitution of two CO ligands by NO+ and PPh3 generates a 1.1 diastereomeric mixture of chiral-at-met
Identification of camphor derivatives as novel M2 ion channel inhibitors of influenza A virus
Zhao, Xin,Zhang, Zhen-Wei,Cui, Wei,Chen, Shengwei,Zhou, Yang,Dong, Jianghong,Jie, Yanling,Wan, Junting,Xu, Yong,Hu, Wenhui
supporting information, p. 727 - 731 (2015/04/27)
Amantadine derivatives have been the only drugs marketed as M2 inhibitors of influenza A for decades. The identification of pinanamine as a novel M2 inhibitor suggests that M2 ion channels can accommodate more types of hydrophobic scaffolds. Herein, we further investigated the M2 ion channels and identified camphor derivatives as new types of M2 inhibitors. Compound 18 was found to be more potent than amantadine against wild-type influenza virus. The molecular docking revealed that compound 18 occupies more space in the M2 ion channel than amantadine and thus exhibits enhanced activity. This journal is
Pinane derivatives
-
, (2008/06/13)
Pinanes substituted by a group X in the 3-position which group is formyl, or its alkyl-acetals or alkyl-hemiacetals, carboxylic acid, carboxylic acid chloride, carboxylic acid amide, hydroxymethyl or aminomethyl substituted in a specific manner at the nitrogen, the optical isomers of these compounds and a process for their manufacture by hydroformylation of α-pinene in the presence of rhodium catalysts, and conversion of the 3-formylpinane first produced into the above derivatives by conventional methods.
