3913-64-2 Usage
Description
[S,(+)]-2-Hydroxypropionaldehyde, also known as (S)-2-Hydroxypropionaldehyde, is a colorless liquid chemical compound with the molecular formula C3H6O2, characterized by a pungent odor. It serves as a versatile intermediate in the synthesis of pharmaceuticals, fragrances, and agricultural chemicals, and is a key building block in the production of 1,3-propanediol, an industrial chemical used in polymers and plastics. Its antimicrobial and antioxidant properties further extend its utility in food preservation and cosmetics.
Uses
Used in Pharmaceutical Industry:
[S,(+)]-2-Hydroxypropionaldehyde is used as an intermediate in the synthesis of various pharmaceutical compounds for its ability to contribute to the development of new drugs.
Used in Fragrance Industry:
[S,(+)]-2-Hydroxypropionaldehyde is used as a component in the creation of fragrance compounds due to its reactive nature and potential to form complex aromatic molecules.
Used in Agricultural Chemical Industry:
[S,(+)]-2-Hydroxypropionaldehyde is used as an intermediate in the production of agricultural chemicals, contributing to the development of effective pest control agents and other agrochemicals.
Used in Polymer and Plastics Industry:
[S,(+)]-2-Hydroxypropionaldehyde is used in the synthesis of 1,3-propanediol, which is an important industrial chemical for the production of polymers and plastics, known for their diverse applications in various consumer and industrial products.
Used in Food Preservation:
[S,(+)]-2-Hydroxypropionaldehyde is used as a preservative in the food industry, leveraging its antimicrobial properties to extend the shelf life of perishable goods.
Used in Cosmetics Industry:
[S,(+)]-2-Hydroxypropionaldehyde is used in cosmetics for its antioxidant properties, helping to prevent the oxidation of ingredients and maintain product stability and efficacy.
Check Digit Verification of cas no
The CAS Registry Mumber 3913-64-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,1 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3913-64:
(6*3)+(5*9)+(4*1)+(3*3)+(2*6)+(1*4)=92
92 % 10 = 2
So 3913-64-2 is a valid CAS Registry Number.
3913-64-2Relevant articles and documents
Structural characterization of an L-fuculose-1-phosphate aldolase from Klebsiella pneumoniae
Lou, Xiaorui,Zhang, Jianyu,Liu, Shimeng,Wang, Runhao,Li, Weiping,Liu, Ruihua,Zhang, Qionglin,Bartlam, Mark
, p. 15 - 19 (2022/04/07)
Fuculose phosphate aldolases play an important role in glycolysis and gluconeogenesis pathways. L-fuculose 1-phosphate aldolase catalyzes the reversible cleavage of L-fuculose 1-phosphate to DHAP and L-lactaldehyde. Class II aldolases found in bacteria are linked to pathogenesis of human pathogens, and have potential applications in the biosynthesis of carbohydrates and other chiral compounds. Here we report the structure of a putative L-fuculose 1-phosphate aldolase (KpFucA) from the nosocomial pathogen Klebsiella pneumoniae to 1.85 ? resolution. The enzyme crystallizes in space group P422 with one monomer per asymmetric unit. Analytical ultracentrifugation analysis confirms that KpFucA is a tetramer in solution. A magnesium ion cofactor and sulfate ion were identified in the active pocket. Enzyme activity assays confirmed that KpFcuA has a strong preference for L-fuculose 1-phosphate as a substrate, but can also catalyze the cleavage of fructose-1,6-bisphosphate and glucose-6-phosphate. This work should provide a starting point for further investigation of the role of KpFucA in K. pneumoniae pathogenesis or in industrial applications.
