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1,2-Benzenediol, 4-(1-hydroxy-2-(methylamino)ethyl)-, (R)-, (R-(R*,R*))-2,3-dihydroxybutanedioate (1:1) (salt) is a complex organic compound with the chemical formula C10H13NO4.C4H6O6. It is a salt formed from the reaction of (R)-1,2-benzenediamine, 4-(1-hydroxy-2-(methylamino)ethyl)-, also known as (R)-N-methyl-1,2-phenylenediamine, and (R-(R*,R*))-2,3-dihydroxybutanedioic acid, commonly referred to as (R,R)-tartaric acid. 1,2-Benzenediol, 4-(1-hydroxy-2-(methylamino)ethyl)-, (R)-, (R-(R*,R*))-2,3-dihydroxybutanedioate (1:1) (salt) is characterized by its chiral nature, with the (R)-enantiomer of the amine and the (R,R)-enantiomer of tartaric acid forming a 1:1 salt. It is an important intermediate in the synthesis of various pharmaceuticals and chemical products, particularly those requiring chiral centers for biological activity.

8028-06-6

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8028-06-6 Usage

Explanation

The compound's full chemical name, which describes its structure and composition.

Explanation

These are alternative names for the compound, which are more commonly used in various contexts.

Explanation

The compound is a salt formed by the combination of two different molecules, which gives it its unique properties.

Explanation

The compound is used in the pharmaceutical industry for a range of applications due to its beneficial properties.

Explanation

The compound has antioxidant properties, which means it can help protect cells from damage caused by free radicals.

Explanation

The compound also possesses anti-inflammatory properties, which can help reduce inflammation in the body.

Explanation

Due to its specific taste, the compound is used as a flavoring agent in certain products, although not widely.

Explanation

The compound has a specific stereochemistry, which refers to the three-dimensional arrangement of its atoms. This stereochemistry is important for its biological activity and properties.

Explanation

The compound is soluble in water, which is an important factor for its pharmaceutical applications and potential use in various formulations.

Explanation

The molecular formula represents the compound's composition in terms of the number of atoms of each element present in a single molecule.

Composition

Salt of 1,2-Benzenediol, 4-(1-hydroxy-2-(methylamino)ethyl)-, (R)and 2,3-dihydroxybutanedioic acid

Pharmaceutical Applications

Various

Antioxidant Properties

Yes

Anti-inflammatory Properties

Yes

Flavoring Agent

Used in some products

Stereochemistry

(R)-(R,R)

Solubility

Soluble in water

Check Digit Verification of cas no

The CAS Registry Mumber 8028-06-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 8,0,2 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 8028-06:
(6*8)+(5*0)+(4*2)+(3*8)+(2*0)+(1*6)=86
86 % 10 = 6
So 8028-06-6 is a valid CAS Registry Number.

8028-06-6Downstream Products

8028-06-6Relevant academic research and scientific papers

PROCESS FOR THE SYNTHESIS OF OPTICALLY ACTIVE BETA-AMINO ALCOHOLS

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Page/Page column 17-18, (2019/11/04)

Subject-matter of the present invention is a process for the preparation of optically active phenyl-beta-amino alcohols by means of a specific reduction of the corresponding phenyl-beta-amino ketones. Further subject-matter of the invention are said novel synthesis intermediates and their use for the preparation of active pharmaceutical ingredients.

PROCESS FOR THE PREPARATION OF OPTICALLY ENRICHED ADRENALINE

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, (2016/06/01)

A process for the production of (-)-adrenaline and (-)-adrenaline-L-tartrate is provided. The process provides for a new, efficient and commercially feasible process for the optical resolution of racemic adrenaline. In one aspect, a one pot process for the synthesis of (-)-adrenaline is provided. The process provides a simple and less expensive 5 process that can be used to prepare commercial scale batches of (-)-adrenaline and (-)-adrenaline-L-tartrate of API quality. The process avoids the use of expensive and unpredictable chiral catalysts.

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