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(2Z,4S,4aR,5S,5aS,11aR,12aR)-2-(amino-hydroxy-methylidene)-11a-chloro-4-dimethylamino-5,10,12a-trihydroxy-6-methylidene-4,4a,5,5a-tetrahydrotetracene-1,3,11,12-tetrone is a complex organic molecule derived from the tetracycline class of antibiotics. It features a tetracycline core structure with various functional groups, including amino, hydroxyl, and methylidene groups, as well as a chlorine atom at position 11a. The presence of these multiple hydroxyl and amino groups suggests its potential for interacting with biological systems and exhibiting pharmacological activity. The chemical structure indicates possible interactions with proteins, nucleic acids, and other biomolecules, making it a molecule of interest for drug development and medicinal chemistry.

55831-75-9

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55831-75-9 Usage

Uses

Used in Pharmaceutical Industry:
(2Z,4S,4aR,5S,5aS,11aR,12aR)-2-(amino-hydroxy-methylidene)-11a-chloro-4-dimethylamino-5,10,12a-trihydroxy-6-methylidene-4,4a,5,5a-tetrahydrotetracene-1,3,11,12-tetrone is used as a broad-spectrum antibiotic for treating various bacterial infections due to its ability to inhibit protein synthesis in bacteria.
Used in Drug Development:
(2Z,4S,4aR,5S,5aS,11aR,12aR)-2-(amino-hydroxy-methylidene)-11a-chloro-4-dimethylamino-5,10,12a-trihydroxy-6-methylidene-4,4a,5,5a-tetrahydrotetracene-1,3,11,12-tetrone is used as a starting material for the development of new drugs with improved properties, such as enhanced antibacterial activity, reduced side effects, or increased bioavailability. Its unique structure and functional groups make it a promising candidate for medicinal chemistry research and the design of novel therapeutic agents.
Used in Medicinal Chemistry Research:
(2Z,4S,4aR,5S,5aS,11aR,12aR)-2-(amino-hydroxy-methylidene)-11a-chloro-4-dimethylamino-5,10,12a-trihydroxy-6-methylidene-4,4a,5,5a-tetrahydrotetracene-1,3,11,12-tetrone is used in medicinal chemistry research to study its interactions with biological targets, such as proteins and nucleic acids. This research can provide insights into its potential pharmacological activity and help guide the development of new drugs with similar structures and mechanisms of action.

Check Digit Verification of cas no

The CAS Registry Mumber 55831-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,3 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55831-75:
(7*5)+(6*5)+(5*8)+(4*3)+(3*1)+(2*7)+(1*5)=139
139 % 10 = 9
So 55831-75-9 is a valid CAS Registry Number.

55831-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S,4aR,5R,5aS,11aR,12aR)-11a-chloro-4-(dimethylamino)-1,5,10,12a-tetrahydroxy-6-methylidene-3,11,12-trioxo-4,4a,5,5a-tetrahydrotetracene-2-carboxamide

1.2 Other means of identification

Product number -
Other names EINECS 259-844-5

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:55831-75-9 SDS

55831-75-9Upstream product

55831-75-9Downstream Products

55831-75-9Relevant academic research and scientific papers

Preparation method of doxycycline intermediate 11 α - chloromethene terramycin (by machine translation)

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Paragraph 0026-0028; 0031-0039, (2020/07/15)

The invention relates to the technical field of veterinary drugs, in particular to a preparation method of a brascomycin intermediate 11 α - chloromethithromycin, which takes 11 α - chlorotetracycline as a raw material, dichloromethane as a solvent, 1, 1 -dichloromethyl - N, N - dimethylamine as a dehydrating agent to obtain 11 α - chloromethithromycin. By means of the preparation method, production potential safety hazards can be reduced, the product yield is high, the generated waste salt is reduced, and the equipment type requirement is reduced. (by machine translation)

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