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127861-96-5

2-(Isopropoxycarbonylmethyl-methyl-sulfamoyl)-benzoic acid isopropyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127861-96-5 Structure

  • Basic information

    1. Product Name: 2-(Isopropoxycarbonylmethyl-methyl-sulfamoyl)-benzoic acid isopropyl ester
    2. Synonyms:
    3. CAS NO:127861-96-5
    4. Molecular Formula:
    5. Molecular Weight: 357.428
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127861-96-5.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: 2-(Isopropoxycarbonylmethyl-methyl-sulfamoyl)-benzoic acid isopropyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(Isopropoxycarbonylmethyl-methyl-sulfamoyl)-benzoic acid isopropyl ester(127861-96-5)
    11. EPA Substance Registry System: 2-(Isopropoxycarbonylmethyl-methyl-sulfamoyl)-benzoic acid isopropyl ester(127861-96-5)

  • 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: 127861-96-5(Hazardous Substances Data)

127861-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127861-96-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,8,6 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 127861-96:
(8*1)+(7*2)+(6*7)+(5*8)+(4*6)+(3*1)+(2*9)+(1*6)=155
155 % 10 = 5
So 127861-96-5 is a valid CAS Registry Number.

127861-96-5Relevant articles and documents

CONDITIONS OF THE DIECKMANN CONDENSATION OF ALKYL 2-(N-METHYL-N-(ALKOXYCARBONYLMETHYL)SULFAMOYL-BENZOATES

Patek, Marcel,Hampl, Frantisek

, p. 3267 - 3277 (2007/10/02)

The Dieckmann condensation of alkyl 2-(N-methyl-N-(alkoxycarbonylmethyl)sulfamoyl)benzoates IIIa-IIIe with various bases affords alkyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxides IVa-IVe which are intermediates in the synthesis of antiinflammatory drug piroxicam.The yields of benzothiazines IVa-IVe depend mostly on the nature of a base, reaction temperature and solvent used for these condensations.Hitherto undescribed esters IIIb-IIIe were sythesized and their structures were confirmed by 1H and 13C NMR, and mass spectra.

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