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CAS

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1078587-17-3

tert-butyl 4-fluorobenzoyl[2-(methylsulfonyl)phenyl]-carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1078587-17-3 Structure

  • Basic information

    1. Product Name: tert-butyl 4-fluorobenzoyl[2-(methylsulfonyl)phenyl]-carbamate
    2. Synonyms: tert-butyl 4-fluorobenzoyl[2-(methylsulfonyl)phenyl]-carbamate
    3. CAS NO:1078587-17-3
    4. Molecular Formula:
    5. Molecular Weight: 393.436
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1078587-17-3.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: tert-butyl 4-fluorobenzoyl[2-(methylsulfonyl)phenyl]-carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl 4-fluorobenzoyl[2-(methylsulfonyl)phenyl]-carbamate(1078587-17-3)
    11. EPA Substance Registry System: tert-butyl 4-fluorobenzoyl[2-(methylsulfonyl)phenyl]-carbamate(1078587-17-3)

  • 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: 1078587-17-3(Hazardous Substances Data)

1078587-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1078587-17-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,8,5,8 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1078587-17:
(9*1)+(8*0)+(7*7)+(6*8)+(5*5)+(4*8)+(3*7)+(2*1)+(1*7)=193
193 % 10 = 3
So 1078587-17-3 is a valid CAS Registry Number.

1078587-17-3Relevant articles and documents

High yield synthesis of 4H-1,4-benzothiazine-1,1-dioxide derivatives

De Montis, Stefania,Fattuoni, Claudia,Cadoni, Enzo,Cabiddu, Maria G.,Usai, Michele,Cabiddu, Salvatore

experimental part, p. 1445 - 1449 (2009/04/07)

(Chemical Equation Presented) 4H-1,4-Benzothiazine-1,1-dioxide derivatives were synthesized through a sequence of almost quantitative reactions. The commercial starting material 2-(methylsulfanyl)aniline was Boc-protected, N-acylated and oxidized at the sulfur atom to obtain a sulfonyl derivative. An anionic transposition of the acyl group followed by a simultaneous deprotection-cyclization gave the title products in excellent yields. All products and intermediates were fully characterized.

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