Cas no 109258-71-1 (Aminolevulinic Acid Related Compound B)

Aminolevulinic Acid Related Compound B is a chemically significant derivative of aminolevulinic acid (ALA), a key intermediate in the biosynthesis of porphyrins and heme. This compound is primarily utilized in research and pharmaceutical applications, particularly in studies involving photodynamic therapy (PDT) and porphyrin metabolism. Its high purity and well-characterized structure make it a reliable reference standard for analytical and synthetic purposes. The compound's stability and compatibility with various experimental conditions further enhance its utility in biochemical and medical research. Researchers value its role in elucidating metabolic pathways and developing novel therapeutic approaches.
Aminolevulinic Acid Related Compound B structure
109258-71-1 structure
Product Name:Aminolevulinic Acid Related Compound B
CAS No:109258-71-1
MF:C14H13NO5
MW:275.256724119186
CID:3064943
PubChem ID:358944
Update Time:2025-11-02

Aminolevulinic Acid Related Compound B Chemical and Physical Properties

Names and Identifiers

    • methyl 5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-oxopentanoate
    • .Methyl 4-oxo-5-phthalimidopentanoate;.methyl 5-phthalimidolevulinate;.5-phthalimidolevulinic acid methyl ester;.4-Oxo-5-phthalimido-valeriansaeure-methylester;.4-oxo-5-phthalimido-valeric acid methyl ester;5-phthalimido-4-oxopentanoic acid methyl ester;
    • 1,3-Dioxo-2-isoindolinelevulinic acid methyl ester
    • Methyl 5-(1,3-dioxoisoindolin-2-yl)-4-oxopentanoate
    • Methyl 5-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-4-oxopentanoate
    • AG-205/09850034
    • SCHEMBL1177477
    • Methyl5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-oxopentanoate
    • CS-0260312
    • Pentanoic acid, 4-oxo-5-phthalimido-, methyl ester
    • Methyl 5-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-oxopentanoate #
    • Aminolevulinic acid Related Compound B
    • methyl 5-phthalimido-4-oxopentanoate
    • 5-phthalimidolevulinic acid methyl ester
    • NSC619109
    • methyl5-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-4-oxopentanoate
    • 109258-71-1
    • methyl 5-(1,3-dioxoisoindol-2-yl)-4-oxopentanoate
    • UNII-59T7E89YHO
    • Methyl phthalimidolevulinate [USP]
    • E80205
    • Z1899649545
    • SR-01000315747-1
    • Oprea1_507211
    • EN300-749183
    • SR-01000315747
    • F8881-7674
    • METHYL PHTHALIMIDOLEVULINATE [USP IMPURITY]
    • Oprea1_628090
    • 59T7E89YHO
    • 2H-Isoindole-2-pentanoic acid, 1,3-dihydro-gamma,1,3-trioxo-, methyl ester
    • STK279558
    • AKOS000583875
    • Methyl phthalimidolevulinate
    • 2H-ISOINDOLE-2-PENTANOIC ACID, 1,3-DIHYDRO-.GAMMA.,1,3-TRIOXO-, METHYL ESTER
    • NSC-619109
    • Methyl phthalimidolevulinate (USP)
    • MFCD00591807
    • 848-270-6
    • METHYL PHTHALIMIDOLEVULINATE (USP IMPURITY)
    • Aminolevulinic Acid Related Compound B
    • Inchi: 1S/C14H13NO5/c1-20-12(17)7-6-9(16)8-15-13(18)10-4-2-3-5-11(10)14(15)19/h2-5H,6-8H2,1H3
    • InChI Key: KFILPVALWMTVMP-UHFFFAOYSA-N
    • SMILES: O=C1C2C=CC=CC=2C(N1CC(CCC(=O)OC)=O)=O

Computed Properties

  • Exact Mass: 275.07900
  • Monoisotopic Mass: 275.079
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 6
  • Complexity: 421
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 80.8A^2
  • XLogP3: 0.4

Experimental Properties

  • PSA: 80.75000
  • LogP: 0.74280

Aminolevulinic Acid Related Compound B Security Information

  • Hazardous Material transportation number:NONH for all modes of transport

Aminolevulinic Acid Related Compound B Pricemore >>

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Additional information on Aminolevulinic Acid Related Compound B

Comprehensive Guide to Aminolevulinic Acid Related Compound B (CAS No. 109258-71-1): Properties, Applications, and Market Insights

Aminolevulinic Acid Related Compound B (CAS No. 109258-71-1) is a derivative of 5-aminolevulinic acid (5-ALA), a naturally occurring compound involved in the heme biosynthesis pathway. This compound has garnered significant attention in recent years due to its potential applications in pharmaceuticals, agriculture, and biochemical research. Researchers and industry professionals frequently search for terms like "Aminolevulinic Acid Related Compound B uses", "CAS 109258-71-1 properties", and "5-ALA derivatives in medicine", reflecting the growing interest in this niche yet impactful chemical.

The molecular structure of Aminolevulinic Acid Related Compound B shares similarities with its parent compound, 5-ALA, but exhibits unique properties that make it suitable for specialized applications. Its chemical formula and exact structure are often studied in relation to photodynamic therapy (PDT), a cutting-edge medical treatment for certain skin conditions. Searches for "photodynamic therapy compounds" and "ALA derivatives in dermatology" highlight the relevance of this compound in modern therapeutic approaches.

In pharmaceutical research, Aminolevulinic Acid Related Compound B is investigated for its role as a precursor in porphyrin synthesis. This biochemical pathway is crucial for understanding cellular metabolism and has implications for developing treatments targeting metabolic disorders. Recent trends show increased interest in queries like "porphyrin biosynthesis intermediates" and "metabolic pathway modulators", indicating the compound's importance in biochemical research.

The agricultural sector has explored Aminolevulinic Acid Related Compound B for its potential as a plant growth regulator. Studies suggest that certain 5-ALA derivatives can enhance chlorophyll production and improve crop yield under specific conditions. This aligns with current searches for "sustainable agriculture chemicals" and "plant growth promoters", reflecting the global shift toward eco-friendly farming solutions.

From a market perspective, the demand for specialized 5-ALA derivatives like Aminolevulinic Acid Related Compound B has shown steady growth, particularly in the pharmaceutical and research sectors. Industry reports correlate with search trends for "specialty chemicals market growth" and "research compound suppliers", suggesting expanding opportunities for manufacturers and distributors of high-purity biochemicals.

Quality control and analytical methods for Aminolevulinic Acid Related Compound B represent another area of professional interest. Advanced techniques such as HPLC and mass spectrometry are commonly employed to ensure purity and verify structural integrity. This technical aspect resonates with laboratory professionals searching for "analytical methods for ALA derivatives" and "chemical characterization techniques".

The stability and storage conditions of Aminolevulinic Acid Related Compound B (CAS No. 109258-71-1) are frequently discussed among researchers. Proper handling protocols and optimal storage temperatures are essential considerations, as evidenced by common queries like "chemical storage best practices" and "stability of research compounds". These practical aspects are crucial for maintaining compound integrity in various research and industrial applications.

Future research directions for Aminolevulinic Acid Related Compound B may explore its potential in novel therapeutic areas and advanced agricultural formulations. The compound's versatility positions it well for emerging applications that align with current scientific trends, including "precision medicine" and "sustainable crop enhancement" - both popular search terms in scientific and industrial communities.

In conclusion, Aminolevulinic Acid Related Compound B (CAS No. 109258-71-1) represents an important biochemical with diverse applications across multiple industries. Its relationship to the fundamental heme biosynthesis pathway and potential modifications make it a valuable subject for ongoing research and development. The compound's relevance is reflected in current search trends and professional inquiries, ensuring its continued importance in scientific and industrial contexts.

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