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  • 1258869-69-0 Structure
  • Basic information

    1. Product Name: C21H31N5O4S
    2. Synonyms: C21H31N5O4S
    3. CAS NO:1258869-69-0
    4. Molecular Formula:
    5. Molecular Weight: 449.574
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1258869-69-0.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: C21H31N5O4S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C21H31N5O4S(1258869-69-0)
    11. EPA Substance Registry System: C21H31N5O4S(1258869-69-0)
  • 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: 1258869-69-0(Hazardous Substances Data)

1258869-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1258869-69-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,8,6 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1258869-69:
(9*1)+(8*2)+(7*5)+(6*8)+(5*8)+(4*6)+(3*9)+(2*6)+(1*9)=220
220 % 10 = 0
So 1258869-69-0 is a valid CAS Registry Number.

1258869-69-0Downstream Products

1258869-69-0Relevant articles and documents

Synthesis and biological activity of novel 1H-1,4-diazepines containing benzene sulfonyl piperazine moiety

Saingar, Shalini,Kumar, Rajesh,Joshi, Yogesh Chandra

, p. 975 - 980 (2012/05/20)

The synthesis of biologically active 1H-1,4-diazepines 6a-e in good yield, from the heterocyclization reaction of [N4-(4-acetylamino) benzene sulfonyl) piperazinyl- N1-propyl]-1,3-dialkyl/aryl propane-1,3-dione 5a-e and ethylenediamine (EDA) in the presence of silica sulphuric acid (SSA) is described. The novel β-diketones/β-ketoesters 5a-e were synthesized by the condensation reaction of [N4-(4- acetylamino) benzene sulfonyl) piperazinyl-N1-1-bromopropane with various β-diketones/β-ketoesters 4a-e.All structures of the newly synthesized compounds were elucidated by elemental analysis and spectral studies.The compounds 6a-e have been screened for antimicrobial, antifungal and anthelmintic activity. Springer Science+Business Media, LLC 2010.

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