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CAS

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1392222-60-4

(S)-3-((tert-butoxycarbonyl)amino)-2-((tert-butyldiphenylsilyl)oxy)propanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1392222-60-4 Structure

  • Basic information

    1. Product Name: (S)-3-((tert-butoxycarbonyl)amino)-2-((tert-butyldiphenylsilyl)oxy)propanoic acid
    2. Synonyms: (S)-3-((tert-butoxycarbonyl)amino)-2-((tert-butyldiphenylsilyl)oxy)propanoic acid
    3. CAS NO:1392222-60-4
    4. Molecular Formula:
    5. Molecular Weight: 443.615
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1392222-60-4.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)-3-((tert-butoxycarbonyl)amino)-2-((tert-butyldiphenylsilyl)oxy)propanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-((tert-butoxycarbonyl)amino)-2-((tert-butyldiphenylsilyl)oxy)propanoic acid(1392222-60-4)
    11. EPA Substance Registry System: (S)-3-((tert-butoxycarbonyl)amino)-2-((tert-butyldiphenylsilyl)oxy)propanoic acid(1392222-60-4)

  • 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: 1392222-60-4(Hazardous Substances Data)

1392222-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1392222-60-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,2,2,2 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1392222-60:
(9*1)+(8*3)+(7*9)+(6*2)+(5*2)+(4*2)+(3*2)+(2*6)+(1*0)=144
144 % 10 = 4
So 1392222-60-4 is a valid CAS Registry Number.

1392222-60-4Relevant articles and documents

Application of the DP4 Probability Method to Flexible Cyclic Peptides with Multiple Independent Stereocenters: The True Structure of Cyclocinamide A

Cooper, Jason K.,Li, Kelin,Aubé, Jeffrey,Coppage, David A.,Konopelski, Joseph P.

, p. 4314 - 4317 (2018/07/29)

A DP4 protocol has been successfully utilized to establish the true structure of the natural product cyclocinamide A, a flexible cyclic peptide with four isolated stereocenters. Benchmarking the necessary level of theory required to successfully predict t

Total synthesis of nominal (11S)- and (11R)-cyclocinamide A

Garcia, Jessica M.,Curzon, Stephanie S.,Watts, Katharine R.,Konopelski, Joseph P.

, p. 2054 - 2057 (2012/06/29)

The cyclocinamides possess a unique β2αβ 2α 14-membered tetrapeptide core. The initially reported biological data and intriguing structure, which was without full stereochemical identification, necessitated synthesis of both nominal (all-S) cyclocinamide A and the 11R isomer. The completed synthesis is highlighted by the use of a (cyclo)asparagine-containing dipeptide as a turn inducing fragment. Due to inconsistencies in analytical data between natural and synthetic samples, a re-evaluation of the natural product stereochemistry appears necessary.

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