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(S)-tert-butyl 3-(2-Hydroxyethyl)piperazine-1-carboxylate is a chemical compound with the molecular formula C13H26N2O3. It is a derivative of piperazine, featuring a tert-butyl group and a hydroxyethyl group. (S)-tert-butyl 3-(2-Hydroxyethyl)piperazine-1-carboxylate is recognized for its role as a chiral building block, which is instrumental in the synthesis of enantiomerically pure compounds. Its unique structure and properties make it a valuable asset in the field of organic synthesis, particularly within the pharmaceutical industry.

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  • (3S)-3-(2-Hydroxyethyl)-1-piperazinecarboxylic acid 1,1-dimethylethyl ester

    Cas No: 1273577-11-9

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  • 1273577-11-9 Structure
  • Basic information

    1. Product Name: (S)-tert-butyl 3-(2-Hydroxyethyl)piperazine-1-carboxylate
    2. Synonyms: (S)-tert-butyl 3-(2-Hydroxyethyl)piperazine-1-carboxylate;(3S)-3-(2-Hydroxyethyl)-1-piperazinecarboxylic acid 1,1-dimethylethyl ester
    3. CAS NO:1273577-11-9
    4. Molecular Formula: C11H22N2O3
    5. Molecular Weight: 230.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1273577-11-9.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: (S)-tert-butyl 3-(2-Hydroxyethyl)piperazine-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-tert-butyl 3-(2-Hydroxyethyl)piperazine-1-carboxylate(1273577-11-9)
    11. EPA Substance Registry System: (S)-tert-butyl 3-(2-Hydroxyethyl)piperazine-1-carboxylate(1273577-11-9)
  • 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: 1273577-11-9(Hazardous Substances Data)

1273577-11-9 Usage

Uses

Used in Pharmaceutical Industry:
(S)-tert-butyl 3-(2-Hydroxyethyl)piperazine-1-carboxylate is used as a chiral building block for the synthesis of complex organic molecules. Its ability to produce enantiomerically pure compounds is crucial in the development of new drugs, where the specific spatial arrangement of atoms can significantly impact the drug's efficacy and safety.
Used in Medicinal Chemistry:
In the realm of medicinal chemistry, (S)-tert-butyl 3-(2-Hydroxyethyl)piperazine-1-carboxylate serves as a key component in the creation of novel pharmaceutical agents. Its unique structural attributes allow for the exploration of new chemical spaces and the potential discovery of innovative therapeutic agents.
Used in Drug Development:
(S)-tert-butyl 3-(2-Hydroxyethyl)piperazine-1-carboxylate is utilized in drug development processes to enhance the synthesis of target compounds with desired biological activities. Its role in creating enantiomerically pure substances ensures that the developed drugs have the intended effects and minimize potential side effects associated with less specific compounds.
Overall, (S)-tert-butyl 3-(2-Hydroxyethyl)piperazine-1-carboxylate is a versatile and essential compound in the synthesis of complex organic molecules, particularly in the pharmaceutical sector, where its chiral properties are harnessed to produce high-quality enantiomerically pure compounds for medicinal applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1273577-11-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,3,5,7 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1273577-11:
(9*1)+(8*2)+(7*7)+(6*3)+(5*5)+(4*7)+(3*7)+(2*1)+(1*1)=169
169 % 10 = 9
So 1273577-11-9 is a valid CAS Registry Number.

1273577-11-9Upstream product

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