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2-amino-4-(4-bromophenyl)-7,7-dimethyl-5-oxo-3-thiocarbamoyl-5,6,7,8-tetrahydro-4H-benzopyran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

117822-66-9

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  • 117822-66-9 Structure

  • Basic information

    1. Product Name: 2-amino-4-(4-bromophenyl)-7,7-dimethyl-5-oxo-3-thiocarbamoyl-5,6,7,8-tetrahydro-4H-benzopyran
    2. Synonyms:
    3. CAS NO:117822-66-9
    4. Molecular Formula:
    5. Molecular Weight: 407.331
    6. EINECS: N/A
    7. Product Categories: N/A

  • 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: 2-amino-4-(4-bromophenyl)-7,7-dimethyl-5-oxo-3-thiocarbamoyl-5,6,7,8-tetrahydro-4H-benzopyran(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-amino-4-(4-bromophenyl)-7,7-dimethyl-5-oxo-3-thiocarbamoyl-5,6,7,8-tetrahydro-4H-benzopyran(117822-66-9)
    11. EPA Substance Registry System: 2-amino-4-(4-bromophenyl)-7,7-dimethyl-5-oxo-3-thiocarbamoyl-5,6,7,8-tetrahydro-4H-benzopyran(117822-66-9)

  • 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: 117822-66-9(Hazardous Substances Data)

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117822-66-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117822-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,8,2 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 117822-66:
(8*1)+(7*1)+(6*7)+(5*8)+(4*2)+(3*2)+(2*6)+(1*6)=129
129 % 10 = 9
So 117822-66-9 is a valid CAS Registry Number.

117822-66-9Relevant academic research and scientific papers

CYCLIZATION REACTIONS OF NITRILES. XXVII. THE STRUCTURE AND CONFORMATIONALLY AMBIDENT HETEROCYCLIZATION OF SUBSTITUTED 2-(THIOCARBAMOYL-2-CYANOETHYL)-3-OXO-1-CYCLOHEXENOLATES

Goncharenko, M. P.,Sharanin, Yu. A.,Shestopalov, A. M.,Litvinov, V. P.,Turov, A. V.

, p. 1362 - 1370 (2007/10/02)

The reaction of arylmethylenecyanoacetamides with dimedone in the presence of bases proceeds with the formation of anti isomers of derivatives of ammonium 2-(2-thiocarbamoyl-2-cyanoethyl)-3-oxo-1-cyclohexen-1-olate.The ambident cyclization of these compou

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