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(4R)-4,5-dihydroxy-2-oxopentanoic acid is a chiral chemical compound with a molecular formula of C5H8O5 and a molar mass of 148.11 g/mol. It is an intermediate in carbohydrate metabolism and plays a role in the biosynthesis of important molecules in the body. (4R)-4,5-dihydroxy-2-oxopentanoic acid also exhibits potential antioxidant and anti-inflammatory properties, making it a valuable subject for research studies.

3495-27-0

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3495-27-0 Usage

Uses

Used in Pharmaceutical Industry:
(4R)-4,5-dihydroxy-2-oxopentanoic acid is used as a precursor in the synthesis of various pharmaceuticals and natural products due to its involvement in the biosynthesis of important molecules in the body.
Used in Research Studies:
(4R)-4,5-dihydroxy-2-oxopentanoic acid is used as a subject of interest in research studies for its potential antioxidant and anti-inflammatory properties, which could lead to the development of new treatments and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 3495-27-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,9 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3495-27:
(6*3)+(5*4)+(4*9)+(3*5)+(2*2)+(1*7)=100
100 % 10 = 0
So 3495-27-0 is a valid CAS Registry Number.

3495-27-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R)-4,5-Dihydroxy-2-oxopentanoic acid

1.2 Other means of identification

Product number -
Other names D-Spinacine

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:3495-27-0 SDS

3495-27-0Downstream Products

3495-27-0Relevant academic research and scientific papers

Syntheses of 2-keto-3-deoxy-D-xylonate and 2-keto-3-deoxy-L-arabinonate as stereochemical probes for demonstrating the metabolic promiscuity of sulfolobus solfataricus towards D-xylose and L-arabinose

Archer, Robert M.,Royer, Sylvain F.,Mahy, William,Winn, Caroline L.,Danson, Michael J.,Bull, Steven D.

, p. 2895 - 2902 (2013)

Practical syntheses of 2-keto-3-deoxy-D-xylonate (D-KDX) and 2-keto-3-deoxy-L-arabinonate (L-KDA) that rely on reaction of the anion of ethyl 2-[(tert-butyldimethylsilyl)oxy]-2-(dimethoxy phosphoryl) acetate with enantiopure glyceraldehyde acetonide, followed by global deprotection of the resultant O-silyl-enol esters, have been developed. This has enabled us to confirm that a 2-keto-3-deoxy-D-gluconate aldolase from the archaeon Sulfolobus solfataricus demonstrates good activity for catalysis of the retro-aldol cleavage of both these enantiomers to afford pyruvate and glycolaldehyde. The stereochemical promiscuity of this aldolase towards these enantiomeric aldol substrates confirms that this organism employs a metabolically promiscuous pathway to catabolise the C5-sugars D-xylose and L-arabinose.

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