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C28H23N3O3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1255216-27-3 Structure
  • Basic information

    1. Product Name: C28H23N3O3S
    2. Synonyms: C28H23N3O3S
    3. CAS NO:1255216-27-3
    4. Molecular Formula:
    5. Molecular Weight: 481.575
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1255216-27-3.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: C28H23N3O3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C28H23N3O3S(1255216-27-3)
    11. EPA Substance Registry System: C28H23N3O3S(1255216-27-3)
  • 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: 1255216-27-3(Hazardous Substances Data)

1255216-27-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1255216-27-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,5,2,1 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1255216-27:
(9*1)+(8*2)+(7*5)+(6*5)+(5*2)+(4*1)+(3*6)+(2*2)+(1*7)=133
133 % 10 = 3
So 1255216-27-3 is a valid CAS Registry Number.

1255216-27-3Downstream Products

1255216-27-3Relevant articles and documents

A versatile one-pot multicomponent synthesis of novel quinazolinon-2-yl- tetrasubstituted thiophenes

Jalani, Hitesh B.,Kaila, Jitendra C.,Baraiya, Arshi B.,Pandya, Amit N.,Sudarsanam,Vasu, Kamala K.

supporting information; experimental part, p. 5686 - 5689 (2010/11/18)

Here, we report a versatile multicomponent synthesis of novel quinazolinon-2-yl-tetrasubstituted thiophenes by a one-pot reaction using different alkyl-3-aminobutenoates, isothiocyanates and 2-halomethyl quinazolinones in good to excellent yields. The reaction probably proceeds by an intramolecular 5-exo-trig cyclisation.

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