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518-12-7

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  • [(7S)-1,2,3,9-tetramethoxy-10-oxo-6,7,8,9-tetrahydro-5H-benzo[a]heptalen-7-yl]carbamic acid

    Cas No: 518-12-7

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518-12-7 Usage

Description

[(7S)-1,2,3,9-tetramethoxy-10-oxo-5,6,7,8,9,10-hexahydrobenzo[a]heptalen-7-yl]carbamic acid is a complex chemical compound characterized by its unique molecular structure. It features a carbamic acid functional group and a heptalen ring system, which is adorned with tetramethoxy and oxo substituents. The presence of a stereocenter at the 7th position, marked as "S," adds to its distinctiveness. [(7S)-1,2,3,9-tetramethoxy-10-oxo-5,6,7,8,9,10-hexahydrobenzo[a]heptalen-7-yl]carbamic acid is synthesized through organic chemistry techniques and holds promise for potential applications in the pharmaceutical and chemical research industries, given its specific structural features and functional groups. Further research and testing are required to explore its properties, possible uses, and safety profile.

Uses

Used in Pharmaceutical Research:
[(7S)-1,2,3,9-tetramethoxy-10-oxo-5,6,7,8,9,10-hexahydrobenzo[a]heptalen-7-yl]carbamic acid is used as a compound in pharmaceutical research for its potential therapeutic applications. Its unique structure and functional groups may offer novel interactions with biological targets, potentially leading to the development of new drugs.
Used in Chemical Research:
In the field of chemical research, [(7S)-1,2,3,9-tetramethoxy-10-oxo-5,6,7,8,9,10-hexahydrobenzo[a]heptalen-7-yl]carbamic acid serves as a subject for studying its reactivity, stability, and the possibility of its use as a building block for more complex molecules or materials.
Used in Drug Synthesis:
[(7S)-1,2,3,9-tetramethoxy-10-oxo-5,6,7,8,9,10-hexahydrobenzo[a]heptalen-7-yl]carbamic acid may be utilized as an intermediate in the synthesis of various drugs, taking advantage of its carbamic acid functional group and the heptalen ring system for creating new pharmacologically active molecules.
Used in Material Science:
Given its structural complexity, [(7S)-1,2,3,9-tetramethoxy-10-oxo-5,6,7,8,9,10-hexahydrobenzo[a]heptalen-7-yl]carbamic acid could be investigated for its potential applications in material science, possibly contributing to the development of new materials with specific properties.
Please note that the specific applications mentioned above are hypothetical and would require further research and validation through scientific experimentation.

Check Digit Verification of cas no

The CAS Registry Mumber 518-12-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 518-12:
(5*5)+(4*1)+(3*8)+(2*1)+(1*2)=57
57 % 10 = 7
So 518-12-7 is a valid CAS Registry Number.

518-12-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Isocolchicine

1.2 Other means of identification

Product number -
Other names -

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:518-12-7 SDS

518-12-7Relevant articles and documents

2,10-DIDEMETHYLCOLCHICINE - A NEW ALKALOID FROM MERENDERA ROBUSTA

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

, p. 58 - 61 (2007/10/02)

The alkaloid complex of Merendera robusta Bge. (family Liliaceae) growing in the Tashkent province of the Uzbek SSR has been investigated.The main alkaloids of this plant are colchicine and colchamine.Eleven tropolone alkaloids and their photochemical isomers have been isolated and identified.A new alkaloid of phenolic nature has been isolated for which the structure of 2,10-didemethylcolchicine has been established.

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