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114991-54-7

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114991-54-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114991-54-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,9,9 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 114991-54:
(8*1)+(7*1)+(6*4)+(5*9)+(4*9)+(3*1)+(2*5)+(1*4)=137
137 % 10 = 7
So 114991-54-7 is a valid CAS Registry Number.

114991-54-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1-trifluoro-N-(6,7,8,9-tetrahydro-5H-carbazol-1-yl)methanesulfonamide

1.2 Other means of identification

Product number -
Other names Methanesulfonamide,N-(2,3,4,9-tetrahydro-1H-carbazol-8-yl)-1,1,1-trifluoro

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:114991-54-7 SDS

114991-54-7Downstream Products

114991-54-7Relevant articles and documents

NUOVI DERIVATI DI 7-AMMINO-2,3-POLIMETILENINDOLI AD ATTIVITA ANTIINFIAMMATORIA

Cerri, R.,Pau, A.,Boatto, G.,Sparatore, F.,Satta, M.,Capasso, F.

, p. 91 - 102 (2007/10/02)

Thirthyfour new N-acylderivatives of 7-amino-2,3-polymethyleneindoles (I) and (II) were prepared and tested, together with a few analogues previously obtained, against carrageenan edema in the rat.Several compounds, at a dose of 1 mmole/kg, exhibit good inhibitory activity, that in some cases is superior to that displayed by indomethacin at a dose of 5 mg/kg.With only one exception, activity is confined to compounds of formula (I) and, generally, derivatives of 2,3-hexamethyleneindole are more active than those of lower homologues.

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