CAS 3927-71-7

(1R)-1-ammonio-2,3-dihydro-1H-indene-1-carboxylate

Description:

(1R)-1-ammonio-2,3-dihydro-1H-indene-1-carboxylate, with the CAS number 3927-71-7, is a chemical compound that features a bicyclic structure characteristic of indene derivatives. This substance contains an ammonium group, which contributes to its solubility in polar solvents and may influence its reactivity and interaction with biological systems. The presence of a carboxylate group indicates that it can participate in acid-base reactions, potentially acting as a weak acid. The stereochemistry denoted by (1R) suggests that the compound has specific spatial arrangements that can affect its biological activity and interactions. Generally, compounds of this nature may exhibit properties relevant to pharmaceuticals or biochemical applications, particularly in the context of drug design or as intermediates in organic synthesis. Its unique structure and functional groups may also allow for various chemical modifications, making it a versatile compound in research and industrial applications.

Formula: C₁₀H₁₁NO₂

InChI: InChI=1/C10H11NO2/c11-10(9(12)13)6-5-7-3-1-2-4-8(7)10/h1-4H,5-6,11H2,(H,12,13)/t10-/m1/s1

SMILES: c1ccc2c(c1)CC[C@@]2(C(=O)O)N

1-amino-2,3-dihydroindene-1-carboxylic acid

CAS: 3927-71-7

Formula: C₁₀H₁₁NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 177.1998

Ref: IN-DA0075C5

1-Aminoindan-1-carboxylic acid

CAS: 3927-71-7

1-Aminoindan-1-carboxylic acid

Purity: 98%

Molecular weight: 177.20g/mol

Ref: 54-OR451226

1-AMINO-2,3-DIHYDRO-1H-INDENE-1-CARBOXYLIC ACID

CAS: 3927-71-7

Formula: C₁₀H₁₁NO₂

Purity: 98%

Molecular weight: 177.203

Ref: 10-F500843

1-Aminoindan-1-carboxylic acid

CAS: 3927-71-7

1-Aminoindan-1-carboxylic acid is a non-competitive inhibitor of the ion channel. It binds to the hydrophobic pocket in the transmembrane domain, where it forms hydrogen bonds with amino acids such as leucine and valine. In vivo studies have shown that 1-aminonindan-1 carboxylic acid can block pentylenetetrazole-, electroshock-, and branched chain induced convulsions in mice. The molecular modeling study showed that 1-aminonindan-1 carboxylic acid binds to the sodium channel, blocking its function by binding to one of two possible sites.

Formula: C₁₀H₁₁NO₂

Purity: Min. 95%

Molecular weight: 177.2 g/mol

Ref: 3D-DAA92771