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2,3-Hexanedione, 1,5,6-trihydroxy-, (S)is a chiral molecule belonging to the hexanedione family of chemicals. It features the specific (S)-configuration and is utilized in the synthesis of various organic compounds and pharmaceuticals. 2,3-Hexanedione, 1,5,6-trihydroxy-, (S)is also recognized for its potential role in the formation of advanced glycation end-products linked to aging and age-related diseases. Furthermore, it has been studied for its antioxidant properties, demonstrating free radical scavenging abilities.

64623-59-2

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64623-59-2 Usage

Uses

Used in Pharmaceutical Industry:
2,3-Hexanedione, 1,5,6-trihydroxy-, (S)is used as an intermediate in the production of pharmaceuticals for its ability to contribute to the synthesis of various organic compounds necessary for drug development.
Used in Chemical Synthesis:
In the chemical industry, 2,3-Hexanedione, 1,5,6-trihydroxy-, (S)is used as a key component in the synthesis of a range of organic compounds, leveraging its unique structure and reactivity.
Used in Antioxidant Applications:
2,3-Hexanedione, 1,5,6-trihydroxy-, (S)is utilized for its antioxidant properties, serving as a free radical scavenger to protect against oxidative stress and potentially contributing to health and wellness applications.
Used in Aging and Age-Related Disease Research:
2,3-Hexanedione, 1,5,6-trihydroxy-, (S)is employed in scientific research to study the formation of advanced glycation end-products, which are implicated in the aging process and the development of age-related diseases, aiding in the understanding and potential treatment of such conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 64623-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,6,2 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64623-59:
(7*6)+(6*4)+(5*6)+(4*2)+(3*3)+(2*5)+(1*9)=132
132 % 10 = 2
So 64623-59-2 is a valid CAS Registry Number.

64623-59-2SDS

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 (5S)-1,5,6-trihydroxyhexane-2,3-dione

1.2 Other means of identification

Product number -
Other names 2,3-Hexanedione,1,5,6-trihydroxy-,(S)

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:64623-59-2 SDS

64623-59-2Upstream product

64623-59-2Downstream Products

64623-59-2Relevant academic research and scientific papers

Radical-Induced Dephosphorylation of Fructose Phosphates in Aqueous Solution

Zegota, Henryk,Sonntag, Clemens von

, p. 1331 - 1337 (2007/10/02)

Oxygen free N2O-saturated aqueous solutions of D-fructose-1-phosphate and D-fructose-6-phosphate were γ-irradiated.Inorganic phosphate and phosphate free sugars (containing four to six carbon atoms) were identified and their G-values measured.D-Fructose-1-phosphate yields (G-values in parentheses) inorganic phosphate (1.6), hexos-2-ulose (0.12), 6-deoxy-2,5-hexodiulose (0.16), tetrulose (0.05) and 3-deoxytetrulose (0.15).D-Fructose-6-phosphate yields inorganic phosphate (1.7), hexos-5-ulose (0.1), 6-deoxy-2,5-hexodiulose (0.36), 3-deoxy-2,5-hexodiulose and 2-deoxyhexos-5-ulose (together 0.18).On treatment with alkaline phosphate further deoxy sugars were recognized and in fructose-1-phosphate G(6-deoxy-2,5-hexodiulose) was increased to a G-value of 0.4.Dephosphorylation is considered to occur mainly after OH attack at C-5 and C-1 in fructose-1-phosphate and at C-5 and C-6 in fructose-6-phosphate.Reaction mechanisms are discussed. - Keywords: D-Fructose-1-phosphate, D-Fructose-6-phosphate, γ-Irradiation; Radical Reactions, Mass Spectrometry

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