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80622-07-7

Nε-Cyclohexyloxycarbonyl-lysin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 80622-07-7 Structure

  • Basic information

    1. Product Name: Nε-Cyclohexyloxycarbonyl-lysin
    2. Synonyms: Nε-Cyclohexyloxycarbonyl-lysin
    3. CAS NO:80622-07-7
    4. Molecular Formula:
    5. Molecular Weight: 272.345
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80622-07-7.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: Nε-Cyclohexyloxycarbonyl-lysin(CAS DataBase Reference)
    10. NIST Chemistry Reference: Nε-Cyclohexyloxycarbonyl-lysin(80622-07-7)
    11. EPA Substance Registry System: Nε-Cyclohexyloxycarbonyl-lysin(80622-07-7)

  • 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: 80622-07-7(Hazardous Substances Data)

80622-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80622-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,2 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 80622-07:
(7*8)+(6*0)+(5*6)+(4*2)+(3*2)+(2*0)+(1*7)=107
107 % 10 = 7
So 80622-07-7 is a valid CAS Registry Number.

80622-07-7Relevant articles and documents

Cyclohexyloxycarbonyl based orthogonal solid phase peptide synthesis in Boc chemistry

Mezo, Gabor,Mihala, Nikolett,Koczan, Gyoergy,Hudecz, Ferenc

, p. 6757 - 6766 (2007/10/03)

Application of N-cyclohexyloxocarbonyl (Choc) protection in Boc chemistry on solid phase provides a new possibility for the preparation of protected peptide fragments. A Choc/OcHex protection scheme allows also the assembly of cyclic lactam peptides linked to the resin through the C- terminus. Choc protection is stable under the 1M TMSOTf-thioanisole/TFA cleavage condition at 0°C, but it is removable by anhydrous HF. We have utilized cyclohexyloxycarbonyl as an orthogonal protecting group for the synthesis of a i) bicyclic epitope peptide of glycoprotein D of HSV 1 on BHA resin and ii) fully protected hexapeptide involved in protein transport on Merrifield resin.

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