CAS 80828-13-3

Octahydroindole-2-Carboxylic Acid

Description:

Octahydroindole-2-carboxylic acid is a bicyclic compound characterized by its unique structure, which includes a saturated indole framework. This compound features a carboxylic acid functional group, which contributes to its acidic properties and potential reactivity. Typically, octahydroindole derivatives exhibit interesting biological activities, making them of interest in medicinal chemistry and drug development. The presence of the carboxylic acid group enhances its solubility in polar solvents and can facilitate interactions with biological targets. Additionally, the saturated nature of the indole ring may influence its conformational flexibility and steric properties, which are crucial for its biological activity. The compound is often studied for its potential applications in pharmaceuticals, particularly in the development of novel therapeutic agents. Safety and handling precautions should be observed, as with any chemical substance, to mitigate risks associated with its use in laboratory settings. Overall, octahydroindole-2-carboxylic acid represents a significant compound in the realm of organic and medicinal chemistry.

Formula: C₉H₁₅NO₂

1H-Indole-2-carboxylic acid, octahydro-, (2a,3ab,7ab)-

CAS: 80828-13-3

Formula: C₉H₁₅NO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 169.2209

Ref: IN-DA00ID4U

rel-(2R,3aR,7aR)-Octahydro-1H-indole-2-carboxylic acid

CAS: 80828-13-3

rel-(2R,3aR,7aR)-Octahydro-1H-indole-2-carboxylic acid

Purity: 95%

Molecular weight: 169.22g/mol

Ref: 54-OR1053472

H-Oic-OH

CAS: 80828-13-3

H-Oic-OH is an enantiopure, stereoselective, chiral molecule that has been used in the synthesis of a cyclohexane ring and allyl carbonate. H-Oic-OH also has a b2 receptor activity and bradykinin b2 binding affinity. H-Oic-OH is an analog for bradykinin b2. The synthesis of H-Oic-OH begins with the reaction of hydrogen chloride and oleum to form hydrochloric acid. This acid is then reacted with allyl alcohol to produce allyl chloride. Allyl chloride can then react with 2 equiv of methyl chloroformate to produce the desired enantiopure, stereoselective, chiral molecule.

Formula: C₉H₁₅NO₂

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 169.22 g/mol

Ref: 3D-FH71796

(2R,3aR,7aR)-rel-OctahydroIndole-2-carboxylic Acid

Controlled Product

CAS: 80828-13-3

Applications (2R,3aR,7aR)-rel-OctahydroIndole-2-carboxylic Acid is a reactant in the preparation of Perindoprilat (P287530), an angiotensin-converting enzyme (ACE) inhibitor. Antihypertensive.
References Blankley, C.J., et. al.: J. Med. Chem., 30, 992 (1987)

Formula: C₉H₁₅NO₂

Color and Shape: Neat

Molecular weight: 169.22

Ref: TR-O236000