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1,3-Diazepino[4,5-b]indol-2(1H)-one,3,4,5,5a,10,10a-hexahydro-7-hydroxy-1,3,5a,10-tetramethyl-, (5aR,10aR)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129263-47-4

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129263-47-4 Usage

Chemical structure

A complex structure consisting of a six-membered diazepine ring fused to an indole ring.

Explanation

The diazepine ring is a six-membered nitrogen-containing ring, and the indole ring is a bicyclic aromatic structure with a benzene ring fused to a pyrrole ring.

Explanation

The stereochemistry of the compound is specified by the (5aR,10aR) configuration, which indicates the spatial arrangement of the atoms at the 5a and 10a positions.

Explanation

The compound has undergone hydrogenation, which means that hydrogen atoms have been added to the molecule, resulting in a fully saturated six-membered diazepine ring and a fully saturated indole ring.

Explanation

Due to its complex structure, the compound has the potential to interact with biological targets, such as proteins or enzymes, which could lead to various biological effects.

Explanation

The intricate structure and potential medicinal properties of the compound make it a candidate for further investigation in the development of new drugs or therapeutic agents.

Explanation

The molecular formula represents the total number of carbon (C), hydrogen (H), nitrogen (N), and oxygen (O) atoms in the molecule.

Explanation

The molecular weight is the sum of the atomic weights of all the atoms in the molecule, which can be used to calculate the mass of a specific quantity of the compound.

Explanation

The solubility of the compound is not provided, but it can be inferred that it may be soluble in certain organic solvents, such as methanol or dimethyl sulfoxide (DMSO), due to its lipophilic nature.

Explanation

The stability of the compound is not provided, but it is likely that it could be sensitive to environmental factors such as light, heat, or moisture, which could affect its shelf life or reactivity.

Stereochemistry

(5aR,10aR)

Hydrogenation

3,4,5,5a,10,10a-hexahydro

Functional groups

Contains a hydroxy group (-OH) and methyl groups (-CH3)

Potential biological activities

May exhibit various biological activities.

Pharmaceutical research interest

May be of interest in pharmaceutical research.

Molecular weight

Approximately 313.38 g/mol

Solubility

Unknown, but may vary depending on the solvent used.

Stability

Unknown, but may be sensitive to light, heat, or moisture.

Check Digit Verification of cas no

The CAS Registry Mumber 129263-47-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,2,6 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129263-47:
(8*1)+(7*2)+(6*9)+(5*2)+(4*6)+(3*3)+(2*4)+(1*7)=134
134 % 10 = 4
So 129263-47-4 is a valid CAS Registry Number.

129263-47-4Downstream Products

129263-47-4Relevant academic research and scientific papers

ISOESERIN UND HOMOISOESERIN. DARSTELLUNG UND STRUKTURAUFKLAERUNG DES INDOLO-1,3-DIAZEPIN-SYSTEMS

Rosenmund, Peter,Gektidis, Simeon,Brill, Hannelore,Kalbe, Renata

, p. 61 - 62 (1989)

A short and efficient synthesis of homoeseroline 5 is described.Isoeserine has the constitution and conformation shown in formula 8.

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