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CAS

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127204-71-1

2-PHENYL-BENZO[D]IMIDAZO[2,1-B]THIAZOLE-3-CARBOXALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127204-71-1 Structure

  • Basic information

    1. Product Name: 2-PHENYL-BENZO[D]IMIDAZO[2,1-B]THIAZOLE-3-CARBOXALDEHYDE
    2. Synonyms: BUTTPARK 9\02-25;IMIDAZO[2,1-B]BENZOTHIAZOLE-3-CARBOXALDEHYDE, 2-PHENYL-;2-PHENYL-BENZO[D]IMIDAZO[2,1-B]THIAZOLE-3-CARBALDEHYDE;2-PHENYL-BENZO[D]IMIDAZO[2,1-B]THIAZOLE-3-CARBOXALDEHYDE
    3. CAS NO:127204-71-1
    4. Molecular Formula: C16H10N2OS
    5. Molecular Weight: 278.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127204-71-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-PHENYL-BENZO[D]IMIDAZO[2,1-B]THIAZOLE-3-CARBOXALDEHYDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-PHENYL-BENZO[D]IMIDAZO[2,1-B]THIAZOLE-3-CARBOXALDEHYDE(127204-71-1)
    11. EPA Substance Registry System: 2-PHENYL-BENZO[D]IMIDAZO[2,1-B]THIAZOLE-3-CARBOXALDEHYDE(127204-71-1)

  • 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: 127204-71-1(Hazardous Substances Data)

127204-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127204-71-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,2,0 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 127204-71:
(8*1)+(7*2)+(6*7)+(5*2)+(4*0)+(3*4)+(2*7)+(1*1)=101
101 % 10 = 1
So 127204-71-1 is a valid CAS Registry Number.

127204-71-1Relevant articles and documents

Metal-free oxidative decarbonylative halogenation of fused imidazoles

Kumar, Gulshan,Shankar, Ravi,Singh, Davinder,Tali, Javeed Ahmad

, p. 20551 - 20555 (2021/11/23)

An efficient strategy has been developed for the deformylative halogenation of carbaldehyde imidazo-fused heterocycles in the presence of TBHP controlled by temperature. A convenient and sequential functionalization (C8 to C3) portrays the synthetic utility of the current method.N-Heterocycle benzamide products were also observedviathe ring opening of imidazopyridines through the cleavage of C-C bond at high temperatures. Features of this method include temperature-controlled excellent regioselectivity, mild conditions and functional group tolerance.

Schiff base imidazo and benzothiazole compound as well as preparation method and application thereof

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Paragraph 0043-0045, (2018/10/19)

The invention relates to schiff base imidazo and benzothiazole compounds as well as a preparation method and application thereof. The compounds are of structures of formulae I to VII as shown in the description. The compounds have certain inhibition activ

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