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  • 1265870-04-9 Structure
  • Basic information

    1. Product Name: C16H20N2S2
    2. Synonyms: C16H20N2S2
    3. CAS NO:1265870-04-9
    4. Molecular Formula:
    5. Molecular Weight: 304.48
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1265870-04-9.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: C16H20N2S2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H20N2S2(1265870-04-9)
    11. EPA Substance Registry System: C16H20N2S2(1265870-04-9)
  • 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: 1265870-04-9(Hazardous Substances Data)

1265870-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1265870-04-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,5,8,7 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1265870-04:
(9*1)+(8*2)+(7*6)+(6*5)+(5*8)+(4*7)+(3*0)+(2*0)+(1*4)=169
169 % 10 = 9
So 1265870-04-9 is a valid CAS Registry Number.

1265870-04-9Downstream Products

1265870-04-9Relevant articles and documents

Synthesis of N-heterocyclic ligands for use in affinity and mixed mode chromatography

Mountford, Simon J.,Campi, Eva M.,Robinson, Andrea J.,Hearn, Milton T.W.

, p. 471 - 485 (2011)

A set of heterocyclic ligands have been synthesised for use in the preparation of mixed mode affinity chromatographic adsorbents for application in the purification of proteins, including antibodies. The ligand structures were designed to consist of a pyridinyl or related aza-heterocyclic nucleus bearing a pendant arm containing either an alkylamine, alkylthiol or hydroxyalkyl nucleophilic group to allow their facile immobilisation onto an activated support matrix. Ligand diversity was achieved by altering the length of the alkyl chain between the heterocyclic nucleus and nucleophilic group, varying the position of alkyl chain attachment to the heterocycle, and incorporating extra substituents into the pyridinyl or related aza-heterocyclic ring. This diversity in ligand structure was intended to enable key structural features of the ligand, required for efficient protein binding, to be determined. In contrast to the previously used multi-step procedures for the preparation of analogous substituted pyridine or aza-heterocyclic compounds, the synthesis routes for the ligands described here have generally utilized very mild, one-step reactions with readily available heterocyclic precursors. Copyright

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