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N4-(Z)-1-(carboxyethyl)cytosine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156998-31-1 Structure
  • Basic information

    1. Product Name: N4-(Z)-1-(carboxyethyl)cytosine
    2. Synonyms: N4-(Z)-1-(carboxyethyl)cytosine
    3. CAS NO:156998-31-1
    4. Molecular Formula:
    5. Molecular Weight: 317.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156998-31-1.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: N4-(Z)-1-(carboxyethyl)cytosine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N4-(Z)-1-(carboxyethyl)cytosine(156998-31-1)
    11. EPA Substance Registry System: N4-(Z)-1-(carboxyethyl)cytosine(156998-31-1)
  • 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: 156998-31-1(Hazardous Substances Data)

156998-31-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156998-31-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,9,9 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 156998-31:
(8*1)+(7*5)+(6*6)+(5*9)+(4*9)+(3*8)+(2*3)+(1*1)=191
191 % 10 = 1
So 156998-31-1 is a valid CAS Registry Number.

156998-31-1Downstream Products

156998-31-1Relevant articles and documents

Structure-activity studies of the binding of modified peptide nucleic acids (PNAs) to DNA

Hyrup, Birgitte,Egholm, Michael,Nielsen, Peter E.,Wittung, Pernilla,Nordén, Bengt,Buchardf, Ole

, p. 7964 - 7970 (1994)

Peptide nucleic acid (PNA) oligomers where one of the repeating backbone units is extended with a methylene group to either N-(2-aminoethyl)-β-alanine or N-(3-aminopropyl)glycine were prepared. Alternatively, the linker to the nucleobase was extended from

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