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H-D-MET(O2)-OH, also known as 2-hydroxy-5-methoxy-2-oxobutanoic acid, is a chemical compound with a molecular formula C5H8O5 and a molecular weight of 148.11 g/mol. It is a derivative of methionine, an essential amino acid involved in protein synthesis and methylation reactions. The "H-D" prefix indicates that it is a D-enantiomer, meaning it has a specific spatial arrangement of atoms. The (O2) notation denotes the presence of a hydroxyl group (-OH) on the second carbon atom of the molecule. H-D-MET(O2)-OH has potential applications in the fields of biochemistry, pharmacology, and medicinal chemistry, particularly in the study of amino acid metabolism and related pathways. Its properties and potential biological activities make it a subject of interest for further research in various scientific disciplines.

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  • 41486-92-4 Structure
  • Basic information

    1. Product Name: H-D-MET(O2)-OH
    2. Synonyms: H-D-MET(O2)-OH;D-Methionine sulfone
    3. CAS NO:41486-92-4
    4. Molecular Formula: C5H11NO4S
    5. Molecular Weight: 181.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 41486-92-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: H-D-MET(O2)-OH(CAS DataBase Reference)
    10. NIST Chemistry Reference: H-D-MET(O2)-OH(41486-92-4)
    11. EPA Substance Registry System: H-D-MET(O2)-OH(41486-92-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 41486-92-4(Hazardous Substances Data)

41486-92-4 Usage

Uses

Used in Biochemistry Research:
H-D-MET(O2)-OH is used as a research compound for studying amino acid metabolism and related pathways. Its unique structure and properties allow scientists to investigate its interactions with enzymes and other biomolecules, providing insights into the regulation of metabolic processes.
Used in Pharmacology:
H-D-MET(O2)-OH is used as a potential therapeutic agent in the development of drugs targeting specific metabolic pathways. Its ability to modulate enzyme activity and influence cellular processes may contribute to the treatment of various diseases and conditions.
Used in Medicinal Chemistry:
H-D-MET(O2)-OH is used as a building block or intermediate in the synthesis of novel compounds with potential medicinal properties. Its unique structure and reactivity make it a valuable component in the design and development of new drugs and pharmaceutical agents.
Used in Nutritional Supplements Industry:
H-D-MET(O2)-OH is used as a dietary supplement to support amino acid metabolism and overall health. Its role in protein synthesis and methylation reactions may contribute to the maintenance of optimal bodily functions and the promotion of well-being.
Used in Cosmetics Industry:
H-D-MET(O2)-OH is used as an active ingredient in cosmetic products for its potential skin health benefits. Its antioxidant properties and ability to modulate cellular processes may contribute to the improvement of skin appearance and the prevention of premature aging.
Used in Food Industry:
H-D-MET(O2)-OH is used as a food additive to enhance the nutritional value of products and support amino acid metabolism. Its presence in food items may contribute to the maintenance of overall health and well-being.

Check Digit Verification of cas no

The CAS Registry Mumber 41486-92-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,8 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41486-92:
(7*4)+(6*1)+(5*4)+(4*8)+(3*6)+(2*9)+(1*2)=124
124 % 10 = 4
So 41486-92-4 is a valid CAS Registry Number.

41486-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-Ammonio-4-(methylsulfonyl)butanoate

1.2 Other means of identification

Product number -
Other names d-Manno-d-heptonsaeureamid

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:41486-92-4 SDS

41486-92-4Relevant articles and documents

Mo(VI) complex catalysed synthesis of sulfonees and their modification for anti-HIV activities

Madduluri, Vimal Kumar,Baig, Noorullah,Chander, Subhash,Murugesan, Sankaranarayanan,Sah, Ajay K.

, (2020/01/23)

An efficient method for the synthesis of sulfones has been developed using sugar derived cis-dioxo molybdenum(VI) complex as catalyst and urea hydrogen peroxide as oxygen source. Present method is highly specific for sulfide oxidation irrespective of presence of alkene and aldehyde groups in the same molecule. Synthesis of fifteen sulfones have been reported with 82–98% isolated yields and the catalyst has been reused five times without any loss in its activity. 2-(Phenylsulfonyl)aniline has been condensed with eight different aromatic aldehydes and the products are being explored for HIV-1 reverse transcriptase inhibition activities.

Homogeneous Aqueous Oxidation of Organic Molecules by OxoneR and Catalysis by a Water-Soluble Manganese Porphyrin Complex

Zheng, Tu-Cai,Richardson, David E.

, p. 833 - 836 (2007/10/02)

Peroxymonosulfate (KHSO5) oxidizes a wide variety of water-soluble organic molecules in aqueous solutions, and the reactions are generally more rapid in phosphate buffer (pH 6-7) than in pure water.A water-soluble porphyrin complex, meso-tetrakis(4-N-methylpyridyl)porphyrinatomanganese(III) chloride, catalyzes epoxidation and hydroxylation under neutral pH conditions.

Manganese Porphyrin Catalyzed Homogeneous Aqueous Oxidation of Organic Molecules by Magnesium Monoperoxyphthalate (MMPP)

Zheng, Tu-Cai,Richardson, David E.

, p. 837 - 840 (2007/10/02)

Magnesium monoperoxyphthalate (MMPP) oxidizes a variety of organic molecules in neutral homogeneous aqueous solutions at room temperature.A water-soluble porphyrin complex, meso-tetrakis-(4-N-methylpyridyl)porhyrinatomanganese(III) chloride, Mn(III)TMPyP(4) Cl, acts as an efficient catalyst for the epoxidation and hydroxylation of water-soluble hydrocarbons.

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