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(+)-5-Vinyl-1,4-dihydro-4-(9H-pyrido[3,4-b]indol-1-ylmethyl)-3-pyridinecarboxylic acid methyl ester is a carboline alkaloid derived from Pauridiantha lyalli Brem. (+)-5-Vinyl-1,4-dihydro-4-(9H-pyrido[3,4-b]indol-1-ylmethyl)-3-pyridinecarboxylic acid methyl ester crystallizes from Et2O and exhibits optical activity with a specific rotation of [α]D578 +650° (c 1.0, CHCI3). Its ultraviolet spectrum in MeOH shows absorption maxima at 235, 284, and 347 nm, indicating its potential for interactions with light and other molecules.

52811-48-0

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52811-48-0 Usage

Uses

Used in Pharmaceutical Industry:
(+)-5-Vinyl-1,4-dihydro-4-(9H-pyrido[3,4-b]indol-1-ylmethyl)-3-pyridinecarboxylic acid methyl ester is used as a pharmaceutical compound for its potential therapeutic applications. The specific rotation and ultraviolet spectrum suggest that it may have unique interactions with biological systems, making it a candidate for further research and development in the field of medicine.
Used in Chemical Research:
In the field of chemical research, (+)-5-Vinyl-1,4-dihydro-4-(9H-pyrido[3,4-b]indol-1-ylmethyl)-3-pyridinecarboxylic acid methyl ester serves as a valuable compound for studying the properties and reactivity of carboline alkaloids. Its crystalline nature and optical activity make it an interesting subject for investigations into the structure-activity relationships and potential applications of similar compounds.
Used in Material Science:
(+)-5-Vinyl-1,4-dihydro-4-(9H-pyrido[3,4-b]indol-1-ylmethyl)-3-pyridinecarboxylic acid methyl ester may also find applications in material science, particularly in the development of novel materials with unique optical, electronic, or mechanical properties. (+)-5-Vinyl-1,4-dihydro-4-(9H-pyrido[3,4-b]indol-1-ylmethyl)-3-pyridinecarboxylic acid methyl ester's absorption maxima in the ultraviolet spectrum could be indicative of its potential use in the creation of light-sensitive materials or devices.

References

Levesque et al., Compt. Rend., 278C, 959 (1974)

Check Digit Verification of cas no

The CAS Registry Mumber 52811-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,1 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52811-48:
(7*5)+(6*2)+(5*8)+(4*1)+(3*1)+(2*4)+(1*8)=110
110 % 10 = 0
So 52811-48-0 is a valid CAS Registry Number.

52811-48-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-[(β-carbolin-1-yl)methyl]-5-vinyl-1,4-dihydropyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names lyanine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:52811-48-0 SDS

52811-48-0Downstream Products

52811-48-0Relevant academic research and scientific papers

Total Synthesis of the Proposed Structures of Indole Alkaloids Lyaline and Lyadine

Bennasar, M.-Lluisa,Roca, Tomas,Monerris, Manuel

, p. 752 - 756 (2007/10/03)

The harman-1,4-dihydropyridines 1 and 2, which constitute the originally proposed structures for the indole alkaloids lyaline and lyadine, have been synthesized, and their NMR data have been compared with those available for the natural products. Due to the discrepancies in the spectral data, the structures of lyadine and lyaline should be revised.

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