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MACULINE is a furoquinoline alkaloid that can be found in Flindersia dissosperrna and F. rnaculosa Lindl. It is a crystalline compound that forms colorless needles when crystallized from methanol (MeOH) or ethanol (EtOH). The base is typically characterized as its hydrochloride salt, with a melting point of 205-210°C (decomposition), which is best obtained from dilute hydrochloric acid (HCl). Additionally, it can be characterized as its picrate salt, with a melting point of 198°C (decomposition). The structure of MACULINE has been determined primarily based on the fragmentation pattern observed in its mass spectrum.

524-89-0

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524-89-0 Usage

Uses

Since the provided materials do not specify any particular applications for MACULINE, it is not possible to list its uses based on the given information. However, as a furoquinoline alkaloid, it may potentially have various applications in fields such as pharmaceuticals, chemistry, or biology, depending on its properties and potential interactions with other compounds. Further research and experimentation would be required to determine its specific uses and applications.

References

Brownetal.,AustraI.J. Chern., 7, 180(1954) Gell, Hughes, Ritchie., ibid, 8,422 (1955) Mass spectrum: Clugston, MacLean., Can. J. Chern., 43, 2516 (1965)

Check Digit Verification of cas no

The CAS Registry Mumber 524-89-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 524-89:
(5*5)+(4*2)+(3*4)+(2*8)+(1*9)=70
70 % 10 = 0
So 524-89-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H9NO4/c1-15-12-7-2-3-16-13(7)14-9-5-11-10(4-8(9)12)17-6-18-11/h2-5H,6H2,1H3

524-89-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Maculine

1.2 Other means of identification

Product number -
Other names Maculin

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:524-89-0 SDS

524-89-0Downstream Products

524-89-0Relevant academic research and scientific papers

Studies on Rutaceae: Part VIII - Chemical Investigation on the Constituents of Atalantia wightii Tanaka, Aegle marmelos Correa ex Koen, Rutea graveolens Linn. and Micromelum pubescens Blume

Banerji, J.,Das, A. K.,Ghoshal, N.,Das, B.

, p. 594 - 596 (2007/10/02)

A new phenolic ester, ethyl p-coumarate (I) and a long chain fatty acid, tetratriacontanoic acid (II) have been obtained from Atalantia wightii Tanaka.Skimmianine (IV) and haplopine (V), two major constituents of Aegle marmelos Corea ex Koen have been tra

An Improved Synthesis of Maculine, a Furoquinoline Alkaloid

Ranade, A. C.,Mali, R. S.,Kurnawal, V. M.

, p. 528 - 529 (2007/10/02)

The improved synthesis of maculine (6) involves lithiation of 2,4-dimethoxy-6,7-methylenedioxyquinoline (2) to give the formyl derivative (3), which on reaction with methoxymethylenetriphenylphosphorane affords a mixture of cis-(4a) and trans-(4b) vinyl ethers.This mixture when heated with 3percent aq.HCl affords the aldehyde (5), which undergoes cyclisation in the presence of PPA to afford 6.

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