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1354-66-1

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1354-66-1 Usage

Description

(6aS)-4,5,6,6a,7,8-Hexahydro-2,11,12-trimethoxy-6-methylbenzo[6,7]cyclohept[1,2,3-ij]isoquinoline-1,10-diol is a complex organic compound with a unique molecular structure. It has been recently reinvestigated by Russian researchers, who have confirmed its empirical formula and structure through NMR and mass spectroscopy. (6aS)-4,5,6,6a,7,8-Hexahydro-2,11,12-trimethoxy-6-methylbenzo[6,7]cyclohept[1,2,3-ij]isoquinoline-1,10-diol is derived from the natural product S-floramultine and has potential applications in various fields due to its unique properties.

Uses

Used in Pharmaceutical Industry:
(6aS)-4,5,6,6a,7,8-Hexahydro-2,11,12-trimethoxy-6-methylbenzo[6,7]cyclohept[1,2,3-ij]isoquinoline-1,10-diol is used as a pharmaceutical compound for its potential therapeutic effects. The compound's unique structure may allow it to interact with specific biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, (6aS)-4,5,6,6a,7,8-Hexahydro-2,11,12-trimethoxy-6-methylbenzo[6,7]cyclohept[1,2,3-ij]isoquinoline-1,10-diol can be used as a starting material for the synthesis of other complex organic molecules. Its unique structure may provide insights into the development of new synthetic pathways and methodologies.
Used in Material Science:
The compound's unique structure and properties may also make it a candidate for use in material science, where it could be explored for potential applications in the development of new materials with specific properties, such as improved conductivity, strength, or stability.
Used in Analytical Chemistry:
(6aS)-4,5,6,6a,7,8-Hexahydro-2,11,12-trimethoxy-6-methylbenzo[6,7]cyclohept[1,2,3-ij]isoquinoline-1,10-diol can be used as a reference compound in analytical chemistry for the development and validation of new analytical methods, such as chromatography or mass spectrometry techniques. Its complex structure and unique properties may help improve the sensitivity and selectivity of these methods.

References

Trozyan, Yusupov, Aslanov., Khirn. Prir. Soedin., 11,527 (1975)

Check Digit Verification of cas no

The CAS Registry Mumber 1354-66-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,3,5 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1354-66:
(6*1)+(5*3)+(4*5)+(3*4)+(2*6)+(1*6)=71
71 % 10 = 1
So 1354-66-1 is a valid CAS Registry Number.

1354-66-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name merenderine

1.2 Other means of identification

Product number -
Other names (S)-Floramultin, Bechuanin

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:1354-66-1 SDS

1354-66-1Upstream product

1354-66-1Downstream Products

1354-66-1Relevant articles and documents

N-OXIDES OF HOMOAPORPHINE ALKALOIDS FROM MERENDERA RADDEANA

Yusupov, M. K.,Chommadov, B. Ch.,Aslanov, Kh. A.

, p. 75 - 79 (2007/10/02)

The alkaloid complex of the leaves, stems, seeds, and seed pods of Merendera raddeana Rgl. (family Liliaceae) has been investigated.A number of known tropolone alkaloids and their photochemical isomers have been isolated together with the homoaporphine bases merenderine, kreysigenine, and O-methylkreysigenine and their N-oxides, which have not been described in the literature.One of them (merenderine N-oxide) has been characterized by its physical constants and has been investigated by IR, PMR, and mass-spectral methods.By a study of the PMR spectrum of the fraction of neutral alkaloids from the leaves of the plant it has been established that it consists mainly of a mixture of equal amounts of colchicine and cornigerine.

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