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(3S,5S,6R)-3-[(3R)-4-Bromo-3-hydroxybutyl]-2-oxo-5,6-diphenyl-4-morpholinecarboxylic Acid tert-Butyl Ester is a complex organic compound characterized by its unique stereochemistry and functional groups. It is an off-white solid with a molecular structure that includes a morpholine ring, phenyl groups, and a bromo-hydroxybutyl side chain. (3S,5S,6R)-3-[(3R)-4-BroMo-3-hydroxybutyl]-2-oxo-5,6-diphenyl-4-Morpholinecarboxylic Acid tert-Butyl Ester is known for its role in the synthesis of enantiopure stereoisomers, which are crucial in various chemical and pharmaceutical applications.

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  • (3S,5S,6R)-3-[(3R)-4-BroMo-3-hydroxybutyl]-2-oxo-5,6-diphenyl-4-Morpholinecarboxylic Acid tert-Butyl Ester

    Cas No: 869111-53-5

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  • 869111-53-5 Structure
  • Basic information

    1. Product Name: (3S,5S,6R)-3-[(3R)-4-BroMo-3-hydroxybutyl]-2-oxo-5,6-diphenyl-4-Morpholinecarboxylic Acid tert-Butyl Ester
    2. Synonyms: (3S,5S,6R)-3-[(3R)-4-BroMo-3-hydroxybutyl]-2-oxo-5,6-diphenyl-4-Morpholinecarboxylic Acid tert-Butyl Ester
    3. CAS NO:869111-53-5
    4. Molecular Formula: C25H30BrNO5
    5. Molecular Weight: 504.4134
    6. EINECS: N/A
    7. Product Categories: Amines, Heterocycles, Pharmaceuticals, Intermediates & Fine Chemicals
    8. Mol File: 869111-53-5.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: Dichloromethane
    9. CAS DataBase Reference: (3S,5S,6R)-3-[(3R)-4-BroMo-3-hydroxybutyl]-2-oxo-5,6-diphenyl-4-Morpholinecarboxylic Acid tert-Butyl Ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3S,5S,6R)-3-[(3R)-4-BroMo-3-hydroxybutyl]-2-oxo-5,6-diphenyl-4-Morpholinecarboxylic Acid tert-Butyl Ester(869111-53-5)
    11. EPA Substance Registry System: (3S,5S,6R)-3-[(3R)-4-BroMo-3-hydroxybutyl]-2-oxo-5,6-diphenyl-4-Morpholinecarboxylic Acid tert-Butyl Ester(869111-53-5)
  • 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: 869111-53-5(Hazardous Substances Data)

869111-53-5 Usage

Uses

Used in Pharmaceutical Industry:
(3S,5S,6R)-3-[(3R)-4-Bromo-3-hydroxybutyl]-2-oxo-5,6-diphenyl-4-morpholinecarboxylic Acid tert-Butyl Ester is used as a reactant in the preparation of enantiopure stereoisomers of hydroxylysinonorleucine and dihydroxylysinonorleucine (D452900). These enantiopure compounds are essential as reduced collagen cross-links, which play a significant role in the development and maintenance of connective tissues in the body. The synthesis of these stereoisomers is crucial for the pharmaceutical industry, as they can be used in the development of drugs targeting various medical conditions related to connective tissue disorders.
Used in Chemical Synthesis:
In the field of chemical synthesis, (3S,5S,6R)-3-[(3R)-4-Bromo-3-hydroxybutyl]-2-oxo-5,6-diphenyl-4-morpholinecarboxylic Acid tert-Butyl Ester serves as an intermediate or building block for the synthesis of more complex organic compounds. Its unique structure and functional groups make it a valuable component in the creation of new molecules with potential applications in various industries, such as materials science, agrochemicals, and specialty chemicals.
Used in Research and Development:
(3S,5S,6R)-3-[(3R)-4-Bromo-3-hydroxybutyl]-2-oxo-5,6-diphenyl-4-morpholinecarboxylic Acid tert-Butyl Ester is also utilized in research and development settings, where scientists explore its properties and potential applications. Its unique stereochemistry and functional groups make it an interesting subject for studies in organic chemistry, asymmetric synthesis, and the development of new synthetic methodologies. Additionally, its potential use in the synthesis of enantiopure compounds makes it a valuable tool for researchers working on chiral chemistry and its applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 869111-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,1,1 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 869111-53:
(8*8)+(7*6)+(6*9)+(5*1)+(4*1)+(3*1)+(2*5)+(1*3)=185
185 % 10 = 5
So 869111-53-5 is a valid CAS Registry Number.

869111-53-5Relevant articles and documents

Reduced collagen cross links: The first synthesis of all the possible (2S,2′S)-stereoisomers of 5-hydroxylysinonorleucine and of 5,5′-dihydroxylysinonorleucine in enantiomerically pure form

Cribiu, Riccardo,Allevi, Pietro,Anastasia, Mario

, p. 3059 - 3069 (2007/10/03)

The paper reports the first enantioselective synthesis of all the possible collagen reduced cross links as described: (2S,2′S,5R)- and (2S,2′S,5S)-5-hydroxylysinonorleucine 3a and 3b, (2S,2′S,5R, 5′R)-5,5′-dihydroxylysinonorleucine 4a, (2S,2′S,5R,5′S)- 5,

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