Cas no 147780-39-0 ((S)-2-Aminohexanedioic Acid 6-Methyl Ester Hydrochloride)

(S)-2-Aminohexanedioic Acid 6-Methyl Ester Hydrochloride is a chiral intermediate used in organic synthesis and pharmaceutical research. Its key advantages include high enantiomeric purity, which is critical for stereoselective reactions, and its esterified carboxyl group, enhancing solubility and reactivity in specific synthetic pathways. The hydrochloride salt form improves stability and handling. This compound is particularly valuable in peptide modification and as a building block for bioactive molecules. Its structural features make it suitable for applications requiring precise chirality control, such as the development of enzyme inhibitors or receptor-targeted drugs. The product is typically supplied with rigorous quality control to ensure consistency in research and industrial processes.
(S)-2-Aminohexanedioic Acid 6-Methyl Ester Hydrochloride structure
147780-39-0 structure
Product Name:(S)-2-Aminohexanedioic Acid 6-Methyl Ester Hydrochloride
CAS No:147780-39-0
MF:C7H14ClNO4
MW:211.643361568451
MDL:MFCD01632070
CID:65065
PubChem ID:24820204
Update Time:2025-11-01

(S)-2-Aminohexanedioic Acid 6-Methyl Ester Hydrochloride Chemical and Physical Properties

Names and Identifiers

    • (S)-2-Amino-6-methoxy-6-oxohexanoic acid hydrochloride
    • L-2-Aminohexanedioic acid 6-methyl ester hydrochloride
    • H-AAD(OME)-OH HCL
    • (S)?-2-?Aminohexanedioic Acid 6-?Methyl Ester Hydrochloride
    • H-Aad(OMe)-OH · HCl
    • H-Aad(OMe)-OH.HC
    • H-Aad(OMe)-OH·HC
    • Hexanedioic acid, 2-amino-, 6-methyl ester, hydrochloride, (S)-
    • L-2-Aminohexanedioicacid-d-methyl ester · HCl
    • L-α-Aminoadipic acid δ-methyl ester hydrochloride
    • H Hcl
    • H-Aad(OMe)-OH
    • H-Aad(OMe)-OH hydrochloride
    • H-HOMOGLU (OME)-OH HCL
    • L-2-AMINOHEXANEDIOICACID-D-METHYL ESTER HYDROCHLORIDE
    • L-2-Aminohexanedioicacid-d-methylesterCl
    • L-Aad(OMe)-OH·HCl
    • L-ALPHA-AMINOADIPIC ACID-DELTA-METHYL ESTER HCL
    • L-2-AMINOHEXANEDIOIC ACID-DELTA-METHYL ESTER HCL
    • (2S)-2-Aminoadipic acid 6-methyl ester hydrochloride
    • H-Aad(OMe)-OHHCl
    • H-Homoglu(ome)-OH-HCl
    • D95453
    • (2S)-2-amino-6-methoxy-6-oxohexanoic acid;hydrochloride
    • BS-21435
    • Hexanedioic acid, 2-amino-, 6-methyl ester, hydrochloride, (S)- (9CI)
    • AKOS007930219
    • SCHEMBL6121574
    • CS-0208907
    • L--Aminoadipic acid--methyl ester HCl;(S)-2-Amino-hexanedioic acid-6-methyl ester HCl;H-Homoglu(OMe)-OH HCl
    • MFCD01632070
    • AKOS015911934
    • H-Aad(OMe)-OH.HCl
    • 147780-39-0
    • L-a-Aminoadipic acid d-methyl ester hydrochloride
    • (2S)-2-AMINO-6-METHOXY-6-OXOHEXANOIC ACID HYDROCHLORIDE
    • O6-Methyl-L-homoglutamic acid HCl
    • IOPRBBKYRZVRBV-JEDNCBNOSA-N
    • (S)-2-Aminohexanedioic Acid 6-Methyl Ester Hydrochloride
    • MDL: MFCD01632070
    • Inchi: 1S/C7H13NO4.ClH/c1-12-6(9)4-2-3-5(8)7(10)11;/h5H,2-4,8H2,1H3,(H,10,11);1H/t5-;/m0./s1
    • InChI Key: IOPRBBKYRZVRBV-JEDNCBNOSA-N
    • SMILES: Cl.O(C)C(CCC[C@@H](C(=O)O)N)=O

Computed Properties

  • Exact Mass: 211.06100
  • Monoisotopic Mass: 211.0611356g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 6
  • Complexity: 169
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 1
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 89.6?2

Experimental Properties

  • PSA: 89.62000
  • LogP: 1.24390

(S)-2-Aminohexanedioic Acid 6-Methyl Ester Hydrochloride Customs Data

  • HS CODE:2922509090
  • Customs Data:

    China Customs Code:

    2922509090

    Overview:

    2922509090. Other amino alcohol phenols\Amino acid phenols and other oxygenated amino compounds. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:AB. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, The color of ethanolamine and its salt should be reported, The package of ethanolamine and its salt shall be declared

    Regulatory conditions:

    A.Customs clearance form for Inbound Goods
    B.Customs clearance form for outbound goods

    Inspection and quarantine category:

    R.Sanitary supervision and inspection of imported food
    S.Sanitary supervision and inspection of exported food

    Summary:

    2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

(S)-2-Aminohexanedioic Acid 6-Methyl Ester Hydrochloride Pricemore >>

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Additional information on (S)-2-Aminohexanedioic Acid 6-Methyl Ester Hydrochloride

Comprehensive Overview of (S)-2-Aminohexanedioic Acid 6-Methyl Ester Hydrochloride (CAS No. 147780-39-0)

(S)-2-Aminohexanedioic Acid 6-Methyl Ester Hydrochloride (CAS No. 147780-39-0) is a specialized chiral compound widely utilized in pharmaceutical research, peptide synthesis, and biochemical applications. This esterified derivative of 2-aminohexanedioic acid features a methyl group at the 6-position, enhancing its solubility and reactivity in organic reactions. The (S)-configuration ensures enantioselectivity, making it valuable for asymmetric synthesis and drug development. Researchers frequently search for "chiral building blocks," "amino acid esters," and "peptide coupling reagents," reflecting its relevance in modern medicinal chemistry.

The compound's hydrochloride salt form improves stability and handling, addressing common challenges in storage and transportation. With the growing demand for "green chemistry" and "sustainable synthesis," (S)-2-Aminohexanedioic Acid 6-Methyl Ester Hydrochloride is often explored for its potential in eco-friendly catalytic processes. Its applications extend to "prodrug design" and "enzyme substrate studies," aligning with trends in personalized medicine and biocatalysis. Analytical techniques like HPLC and NMR are critical for quality control, ensuring compliance with industry standards.

In the context of "drug delivery systems," this compound's ester moiety offers tunable release kinetics, a hot topic in nanomedicine. Its structural similarity to natural amino acids also makes it a candidate for "biomimetic materials." Recent publications highlight its role in "metal-organic frameworks (MOFs)" for controlled release, resonating with searches for "advanced drug carriers." The CAS No. 147780-39-0 is frequently cross-referenced in patents related to "targeted therapy" and "bioconjugation."

From a synthetic perspective, the compound's methyl ester group facilitates straightforward derivatization, a key advantage for "high-throughput screening" libraries. Its compatibility with "solid-phase peptide synthesis (SPPS)" answers frequent queries about "peptide modification tools." As the pharmaceutical industry shifts toward "continuous manufacturing," intermediates like (S)-2-Aminohexanedioic Acid 6-Methyl Ester Hydrochloride gain traction for scalability and reproducibility.

Safety and regulatory aspects are equally critical. While not classified as hazardous, proper handling under "GMP guidelines" is recommended. The compound's "structure-activity relationship (SAR)" data is often sought for "computational chemistry" models, bridging gaps between in silico predictions and experimental validation. Its role in "metabolomics studies" further underscores its interdisciplinary utility.

In summary, (S)-2-Aminohexanedioic Acid 6-Methyl Ester Hydrochloride (CAS No. 147780-39-0) is a versatile chiral synthon with expanding applications in drug discovery and biomaterials. Its alignment with trends like "precision medicine" and "catalysis innovation" ensures sustained interest across academic and industrial sectors.

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