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CAS

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1067659-00-0

tert-butyl methyl((S)-azepan-2-one-3-ylamino-(R)-oxo-3-phenylpropan-2-yl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1067659-00-0 Structure

  • Basic information

    1. Product Name: tert-butyl methyl((S)-azepan-2-one-3-ylamino-(R)-oxo-3-phenylpropan-2-yl)carbamate
    2. Synonyms: tert-butyl methyl((S)-azepan-2-one-3-ylamino-(R)-oxo-3-phenylpropan-2-yl)carbamate
    3. CAS NO:1067659-00-0
    4. Molecular Formula:
    5. Molecular Weight: 389.495
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1067659-00-0.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: tert-butyl methyl((S)-azepan-2-one-3-ylamino-(R)-oxo-3-phenylpropan-2-yl)carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl methyl((S)-azepan-2-one-3-ylamino-(R)-oxo-3-phenylpropan-2-yl)carbamate(1067659-00-0)
    11. EPA Substance Registry System: tert-butyl methyl((S)-azepan-2-one-3-ylamino-(R)-oxo-3-phenylpropan-2-yl)carbamate(1067659-00-0)

  • 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: 1067659-00-0(Hazardous Substances Data)

1067659-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1067659-00-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,7,6,5 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1067659-00:
(9*1)+(8*0)+(7*6)+(6*7)+(5*6)+(4*5)+(3*9)+(2*0)+(1*0)=170
170 % 10 = 0
So 1067659-00-0 is a valid CAS Registry Number.

1067659-00-0Relevant articles and documents

Resolution of the Confusion in the Assignments of Configuration for the Ciliatamides, Acylated Dipeptides from Marine Sponges

Takada, Kentaro,Irie, Raku,Suo, Rei,Matsunaga, Shigeki

, p. 2845 - 2849 (2017/11/06)

Direct comparison of authentic ciliatamide A with four synthetic isomers (1-4) by means of NMR and chiral-phase HPLC revealed that ciliatamide A possesses the 12R (d-N-MePhe residue) and 22S (l-Lys residue) configurations, which were not identical with either our previous assignment or those proposed by others through total synthesis. The absolute configuration of the methionine sulfoxide residue in ciliatamide D was also revised to be d.

Total synthesis of ciliatamides A-C: Stereochemical revision and the natural product-guided synthesis of unnatural analogs

Lewis, Jana A.,Daniels, R. Nathan,Lindsley, Craig W.

supporting information; experimental part, p. 4545 - 4548 (2009/05/27)

(Chemical Equation Presented) The first total synthesis of Ciliatamides A-C was completed, leading to a revision of the reported stereochemistry from (S,S) to the (R,R) enantiomers. Due to the expedited route, a library of over 50 unnatural ciliatamide analogs was also prepared.

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