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79848-46-7

(S)-2-Benzyloxycarbonylamino-4-((S)-2-oxo-tetrahydro-furan-3-ylamino)-butyric acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 79848-46-7 Structure

  • Basic information

    1. Product Name: (S)-2-Benzyloxycarbonylamino-4-((S)-2-oxo-tetrahydro-furan-3-ylamino)-butyric acid tert-butyl ester
    2. Synonyms:
    3. CAS NO:79848-46-7
    4. Molecular Formula:
    5. Molecular Weight: 392.452
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 79848-46-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-2-Benzyloxycarbonylamino-4-((S)-2-oxo-tetrahydro-furan-3-ylamino)-butyric acid tert-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-2-Benzyloxycarbonylamino-4-((S)-2-oxo-tetrahydro-furan-3-ylamino)-butyric acid tert-butyl ester(79848-46-7)
    11. EPA Substance Registry System: (S)-2-Benzyloxycarbonylamino-4-((S)-2-oxo-tetrahydro-furan-3-ylamino)-butyric acid tert-butyl ester(79848-46-7)

  • 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: 79848-46-7(Hazardous Substances Data)

79848-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79848-46-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,4 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79848-46:
(7*7)+(6*9)+(5*8)+(4*4)+(3*8)+(2*4)+(1*6)=197
197 % 10 = 7
So 79848-46-7 is a valid CAS Registry Number.

79848-46-7Downstream Products

79848-46-7Relevant articles and documents

SYNTHESIS OF AVENIC ACID A AND 2'-DEOXYMUGIENIC ACID, AMINO ACIDS POSSESSING AN IRON CHELATING ACTIVITY

Fushiya, Shinji,Sato, Yoshikazu,Nakatsuyama, Shuichi,Kanuma, Norio,Nozoe, Shigeo

, p. 909 - 912 (1981)

Avenic acid A (1), an amino acid derivative possessing an iron chelating activity and excreted from the root of Avena sativa L. was synthesized in optically active form by successive reductive coupling of protected L-aspartic β-semialdehyde and L-malic semialdehyde with L-homoserine lactone. 2'-Deoxymugineic acid (2), a related substance was also synthesized by the same method by which the stereostructure of this amino acid derivative was proved to be 2(S), 3'(S),3''(S)-N--azetidine-2-carboxylic acid.

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