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104761-70-8

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104761-70-8 Usage

Description

(7R,12S)-10-fluoro-7,12-dimethyl-1,2,3,4,7,12-hexahydrotetraphene-7,12-diol is a complex organic molecule characterized by a fluorine atom attached to the 10th position of a carbon chain, along with hydroxyl groups at the 7th and 12th positions. It features a unique ring structure with seven and twelve members, and two methyl groups are attached to the 7th and 12th positions. (7R,12S)-10-fluoro-7,12-dimethyl-1,2,3,4,7,12-hexahydrotetraphene-7,12-diol may hold potential applications in various fields, including medicine, pharmaceuticals, and chemical synthesis, making it a subject of interest for further research and development.

Uses

Used in Pharmaceutical Industry:
(7R,12S)-10-fluoro-7,12-dimethyl-1,2,3,4,7,12-hexahydrotetraphene-7,12-diol is used as a potential pharmaceutical compound for its unique molecular structure and properties, which may contribute to the development of new drugs and therapies.
Used in Chemical Synthesis:
In the chemical synthesis industry, (7R,12S)-10-fluoro-7,12-dimethyl-1,2,3,4,7,12-hexahydrotetraphene-7,12-diol can be utilized as a key intermediate or building block in the creation of more complex molecules and materials.
Used in Medicinal Research:
(7R,12S)-10-fluoro-7,12-dimethyl-1,2,3,4,7,12-hexahydrotetraphene-7,12-diol is employed in medicinal research for its potential to contribute to the understanding of molecular interactions and the development of novel therapeutic agents.
Note: The specific applications and industries listed above are inferred based on the general potential of the compound as described in the provided materials. The actual uses may vary and would require further research and development to confirm.

Check Digit Verification of cas no

The CAS Registry Mumber 104761-70-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,6 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 104761-70:
(8*1)+(7*0)+(6*4)+(5*7)+(4*6)+(3*1)+(2*7)+(1*0)=108
108 % 10 = 8
So 104761-70-8 is a valid CAS Registry Number.

104761-70-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (7R,12S)-10-fluoro-7,12-dimethyl-1,2,3,4-tetrahydrobenzo[a]anthracene-7,12-diol

1.2 Other means of identification

Product number -
Other names 10-fluoro-1,2,3,4,7,12-hexahydro-7,12-dimethylbenz<a>anthracene-7,12-diol

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:104761-70-8 SDS

104761-70-8Relevant articles and documents

The 5-, 6-, and 10-Fluoro-1,2,3,4-tetrahydro-7,12-dimethylbenzanthracenes. Comparative Acid-Catalyzed Isomerization to Exo Methylene Tautomers: A 6-Fluoro Peri Effect

Witiak, Donald T.,Abood, Norman A.,Goswami, Shyamaprosad,Milo, George E.

, p. 4499 - 4507 (2007/10/02)

Syntheses for 5-, 6-, and 10-fluoro-1,2,3,4-tetrahydro-7,12-dimethylbenzanthracenes (3-5) from an aminotetralin-HCl 6, fluorotetralin 14, and tetrahydronaphthaldehyde 29, respectively, are described.Comparative acid-catalyzed isomerization studies in refluxing benzene revealed that the 6-F analogue 4 equilibrates with 12- and 7-methylene tautomers 20 and 21 within 1 h.When the 12-methylene tautomer 20 was treated with p-toluenesulfonic acid in refluxing benzene the thermodynamic product ratio (4/20/21 = 1.0:0.6:2.8) was obtained after 72 h.These data are markedlydifferent than results observed for acid-catalyzed isomerization of 1,2,3,4-tetrahydro-7,12-dimethylbenzanthracene (TH-DMBA, 1), 5F-TH-DMBA (3) or 10F-TH-DMBA (5) which after 72 h only afforded aryl to 7-methylene isomer ratios of 14:1, 8:1 and 8:1, respectively.The additional peri interaction between the 7-CH3 and 6-F functions of 4 serves as explanation for the facile acid-catalyzed isomerization of 4 to the sterically least crowded, thermodynamically more stable 7-methylene tautomer 21.

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