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3-Pyrrolidinecarboxylic acid, 4-(4-methoxyphenyl)-, methyl ester, (3S,4R)is a chiral chemical compound with the molecular formula C15H19NO3. It is a methyl ester derivative of 3-pyrrolidinecarboxylic acid and 4-(4-methoxyphenyl), existing in two stereoisomeric forms, (3S,4R)and (3R,4S)-. 3-Pyrrolidinecarboxylic acid, 4-(4-methoxyphenyl)-, methyl ester, (3S,4R)is known for its potential medicinal properties and is utilized as a chiral building block in the synthesis of pharmaceutical drugs and biologically active molecules.

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  • 1269260-01-6 Structure
  • Basic information

    1. Product Name: 3-Pyrrolidinecarboxylic acid, 4-(4-methoxyphenyl)-, methyl ester, (3S,4R)-
    2. Synonyms: 3-Pyrrolidinecarboxylic acid, 4-(4-methoxyphenyl)-, methyl ester, (3S,4R)-
    3. CAS NO:1269260-01-6
    4. Molecular Formula: C13H17NO3
    5. Molecular Weight: 235.27898
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1269260-01-6.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: 3-Pyrrolidinecarboxylic acid, 4-(4-methoxyphenyl)-, methyl ester, (3S,4R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Pyrrolidinecarboxylic acid, 4-(4-methoxyphenyl)-, methyl ester, (3S,4R)-(1269260-01-6)
    11. EPA Substance Registry System: 3-Pyrrolidinecarboxylic acid, 4-(4-methoxyphenyl)-, methyl ester, (3S,4R)-(1269260-01-6)
  • 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: 1269260-01-6(Hazardous Substances Data)

1269260-01-6 Usage

Uses

Used in Pharmaceutical Industry:
3-Pyrrolidinecarboxylic acid, 4-(4-methoxyphenyl)-, methyl ester, (3S,4R)is used as a chiral building block for the synthesis of various pharmaceutical drugs and biologically active molecules. Its unique stereochemistry allows for the creation of enantiomerically pure compounds, which is crucial for the development of effective and safe medications.
Used in Organic Chemical Synthesis:
In the field of organic chemistry, 3-Pyrrolidinecarboxylic acid, 4-(4-methoxyphenyl)-, methyl ester, (3S,4R)serves as a valuable reagent for the preparation of various organic compounds. Its versatile structure and functional groups enable chemists to perform a range of reactions, leading to the formation of new molecules with potential applications in various industries.
Used in Medicinal Chemistry Research:
3-Pyrrolidinecarboxylic acid, 4-(4-methoxyphenyl)-, methyl ester, (3S,4R)is being studied for its pharmacological activities, as it possesses potential medicinal properties. Researchers are exploring its interactions with biological targets and evaluating its efficacy in treating various diseases and conditions. 3-Pyrrolidinecarboxylic acid, 4-(4-methoxyphenyl)-, methyl ester, (3S,4R)-'s unique structure and chirality make it an interesting candidate for drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 1269260-01-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,9,2,6 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1269260-01:
(9*1)+(8*2)+(7*6)+(6*9)+(5*2)+(4*6)+(3*0)+(2*0)+(1*1)=156
156 % 10 = 6
So 1269260-01-6 is a valid CAS Registry Number.

1269260-01-6Downstream Products

1269260-01-6Relevant articles and documents

HETEROCYCLIC COMPOUNDS FOR MODULATING NR2F6

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Paragraph 00399; 00415, (2021/09/04)

The present disclosure relates to compounds capable of modulating the activity of NR2F6. The compounds of the disclosure may be used in methods for the prevention and/or the treatment of diseases and disorders associated with modulating NR2F6 activity.

Design and syntheses of melanocortin subtype-4 receptor agonists. Part 2: Discovery of the dihydropyridazinone motif

Ujjainwalla, Feroze,Warner, Daniel,Snedden, Christine,Grisson, Ricky D.,Walsh, Thomas F.,Wyvratt, Matthew J.,Kalyani, Rubana N.,MacNeil, Tanya,Tang, Rui,Weinberg, David H.,Van Der Ploeg, Lex,Goulet, Mark T.

, p. 4023 - 4028 (2007/10/03)

Optimization of the biological activity of a new class of non-peptidyl, pyridazinone derived human melanocortin subtype-4 receptor agonists is disclosed.

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