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1579275-63-0

(2R,3R)-tert-butyl 2-benzyloxycarbonylamino-3-tert-butoxycarbonylaminobutanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1579275-63-0 Structure

  • Basic information

    1. Product Name: (2R,3R)-tert-butyl 2-benzyloxycarbonylamino-3-tert-butoxycarbonylaminobutanoate
    2. Synonyms:
    3. CAS NO:1579275-63-0
    4. Molecular Formula:
    5. Molecular Weight: 408.495
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1579275-63-0.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: (2R,3R)-tert-butyl 2-benzyloxycarbonylamino-3-tert-butoxycarbonylaminobutanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3R)-tert-butyl 2-benzyloxycarbonylamino-3-tert-butoxycarbonylaminobutanoate(1579275-63-0)
    11. EPA Substance Registry System: (2R,3R)-tert-butyl 2-benzyloxycarbonylamino-3-tert-butoxycarbonylaminobutanoate(1579275-63-0)

  • 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: 1579275-63-0(Hazardous Substances Data)

1579275-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1579275-63-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,9,2,7 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1579275-63:
(9*1)+(8*5)+(7*7)+(6*9)+(5*2)+(4*7)+(3*5)+(2*6)+(1*3)=220
220 % 10 = 0
So 1579275-63-0 is a valid CAS Registry Number.

1579275-63-0Relevant articles and documents

Synthesis and biological evaluation of quinaldopeptin

Katayama, Katsushi,Okamura, Takuya,Sunadome, Takuya,Nakagawa, Koji,Takeda, Hiroshi,Shiro, Motoo,Matsuda, Akira,Ichikawa, Satoshi

, p. 2580 - 2590 (2014/04/17)

The second-generation total synthesis of quinaldopeptin (1) was established via a Staudinger/aza-Wittig/diastereoselective Ugi three-component reaction sequence and a racemization-free [5 + 5] coupling and macrolactamization. A single-crystal X-ray structure of the chromophore analogue 26 confirmed the structural and stereochemical assignments of the macrocycle. Synthetic 1 successfully unwound supercoiled DNA to form a relaxed DNA in a dose-dependent manner, the binding affinity of 1 to four dsODNs was within a similar range (Kb = 1.45-2.53 × 107 M-1), and the sequence selectivity was subtle. It was suggested that 1 possesses biological behaviors similar to those of sandramycin (2) in terms of cytotoxic activity against human cancer cell lines (IC50 = 3.2-12 nM) and HIF-1 inhibitory activity.

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