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CAS

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273757-03-2

(S)-3-IMidazo[4,5-b]pyridin-3-yl-pyrrolidine-1-carboxylic acid tert-butyl ester is a pyrrolidine derivative featuring a tert-butyl ester functional group and a specific (S)-stereochemistry. (S)-3-IMidazo[4,5-b]pyridin-3-yl-pyrrolidine-1-carboxylic acid tert-butyl ester consists of an imidazo[4,5-b]pyridine ring system, a pyrrolidine ring, and a carboxylic acid functional group, with the tert-butyl ester acting as a protective group in organic synthesis. Its unique structure and functional groups may grant it potential applications in medicinal chemistry, organic synthesis, and materials science, although further research and experimentation are required to ascertain its specific properties and uses.

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  • (S)-3-IMidazo[4,5-b]pyridin-3-yl-pyrrolidine-1-carboxylic acid tert-butyl ester

    Cas No: 273757-03-2

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  • 273757-03-2 Structure

  • Basic information

    1. Product Name: (S)-3-IMidazo[4,5-b]pyridin-3-yl-pyrrolidine-1-carboxylic acid tert-butyl ester
    2. Synonyms: (S)-3-IMidazo[4,5-b]pyridin-3-yl-pyrrolidine-1-carboxylic acid tert-butyl ester;(S)-tert-Butyl 3-(3H-iMidazo[4,5-b]pyridin-3-yl)pyrrolidine-1-carboxylate
    3. CAS NO:273757-03-2
    4. Molecular Formula: C15H20N4O2
    5. Molecular Weight: 288.3449
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 273757-03-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 445.9±55.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.27±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 5.60±0.30(Predicted)
    10. CAS DataBase Reference: (S)-3-IMidazo[4,5-b]pyridin-3-yl-pyrrolidine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
    11. NIST Chemistry Reference: (S)-3-IMidazo[4,5-b]pyridin-3-yl-pyrrolidine-1-carboxylic acid tert-butyl ester(273757-03-2)
    12. EPA Substance Registry System: (S)-3-IMidazo[4,5-b]pyridin-3-yl-pyrrolidine-1-carboxylic acid tert-butyl ester(273757-03-2)

  • 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: 273757-03-2(Hazardous Substances Data)

273757-03-2 Usage

Uses

Used in Medicinal Chemistry:
(S)-3-IMidazo[4,5-b]pyridin-3-yl-pyrrolidine-1-carboxylic acid tert-butyl ester is used as a chemical intermediate for the development of new pharmaceuticals, leveraging its unique structure and functional groups to create novel drug candidates.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-3-IMidazo[4,5-b]pyridin-3-yl-pyrrolidine-1-carboxylic acid tert-butyl ester serves as a key building block for the synthesis of more complex molecules, taking advantage of its reactive sites and protecting group.
Used in Materials Science:
(S)-3-IMidazo[4,5-b]pyridin-3-yl-pyrrolidine-1-carboxylic acid tert-butyl ester is used as a component in the development of advanced materials, potentially contributing to the creation of new polymers, coatings, or other material innovations due to its structural and functional characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 273757-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,3,7,5 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 273757-03:
(8*2)+(7*7)+(6*3)+(5*7)+(4*5)+(3*7)+(2*0)+(1*3)=162
162 % 10 = 2
So 273757-03-2 is a valid CAS Registry Number.

273757-03-2Downstream Products

273757-03-2Relevant articles and documents

S-3578, A new broad spectrum parenteral cephalosporin exhibiting potent activity against both methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa synthesis and structure-activity relationships

Yoshizawa, Hidenori,Itani, Hikaru,Ishikura, Koji,Irie, Tadashi,Yokoo, Katsuki,Kubota, Tadatoshi,Minami, Kyoji,Iwaki, Tsutomu,Miwa, Hideaki,Nishitani, Yasuhiro

, p. 975 - 992 (2007/10/03)

A series of 7-aminothiadiazolylcephalosporins having a 1-(substituted)-1H-imidazo[4,5-b]pyridinium group at the C-3′ position of the cephem nucleus were synthesized and evaluated for in vitro antibacterial activities. Among the cephalosporins prepared in

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