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CAS

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1574185-26-4

benzyl N-(6,7-dimethoxy-1,2,3,4-tetrahydronaphthalen-1-yl)sulphamoylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1574185-26-4 Structure

  • Basic information

    1. Product Name: benzyl N-(6,7-dimethoxy-1,2,3,4-tetrahydronaphthalen-1-yl)sulphamoylcarbamate
    2. Synonyms: benzyl N-(6,7-dimethoxy-1,2,3,4-tetrahydronaphthalen-1-yl)sulphamoylcarbamate
    3. CAS NO:1574185-26-4
    4. Molecular Formula:
    5. Molecular Weight: 420.486
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1574185-26-4.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: benzyl N-(6,7-dimethoxy-1,2,3,4-tetrahydronaphthalen-1-yl)sulphamoylcarbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl N-(6,7-dimethoxy-1,2,3,4-tetrahydronaphthalen-1-yl)sulphamoylcarbamate(1574185-26-4)
    11. EPA Substance Registry System: benzyl N-(6,7-dimethoxy-1,2,3,4-tetrahydronaphthalen-1-yl)sulphamoylcarbamate(1574185-26-4)

  • 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: 1574185-26-4(Hazardous Substances Data)

1574185-26-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1574185-26-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,4,1,8 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1574185-26:
(9*1)+(8*5)+(7*7)+(6*4)+(5*1)+(4*8)+(3*5)+(2*2)+(1*6)=184
184 % 10 = 4
So 1574185-26-4 is a valid CAS Registry Number.

1574185-26-4Downstream Products

1574185-26-4Relevant articles and documents

Novel sulphamides and sulphonamides incorporating the tetralin scaffold as carbonic anhydrase and acetylcholine esterase inhibitors

Akincioglu, Akin,Topal, Meryem,Guelcin, Ilhami,Goeksu, Sueleyman

, p. 68 - 76 (2014/01/23)

Reactions of amino, aminomethyl tetralins and benzyl alcohol with chlorosulphonyl isocyanate (CSI) afforded sulphamoyl carbamates. The sulphamoyl carbamates were converted to sulphamides by palladium-catalysed hydrogenolysis. Sulphonamides were synthesize

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