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61509-78-2

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61509-78-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61509-78-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,0 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61509-78:
(7*6)+(6*1)+(5*5)+(4*0)+(3*9)+(2*7)+(1*8)=122
122 % 10 = 2
So 61509-78-2 is a valid CAS Registry Number.

61509-78-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-anilino-N,N-dimethylnaphthalene-2-sulfonamide

1.2 Other means of identification

Product number -
Other names 6-N-phenylamino-2-naphthalenesulfon-N,N-dimethylamide

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:61509-78-2 SDS

61509-78-2Downstream Products

61509-78-2Relevant articles and documents

INTRAMOLECULAR DONOR-ACCEPTOR SYSTEMS. Part 8. Solvent and substituent effects on the fluorescence emission of 6-N-methyl-N-phenylamino-2-naphthalenesulfon-N,N-dimethylamides

Kosower, Edward M.,Kanety, Hannah

, p. 259 - 268 (2007/10/02)

The dual fluorescence (emissions from S1,np and S1,ct states) of N-phenylaminonaphthalenesulfonate (ANS) systems is briefly reviewed.The 6-N-methyl-N-phenylamino-2-naphthalenesulfon-N,N-dimethylamides also exhibit dual fluorescence, as shown by plots of emission energy and ΦF against the sovent polarity parameter, ET(30).The solvent polarities, for which appearance of S1,ct emission marks the occurence of an intramolecular electron transfer (i.e.t.) process, are appreciably lower than those of the corresponding sulfonates.The fluorescence of the dimethylamides exhibits a high sensitivity to substituent change, the apparent Hammett ρ value being ca. -13 for unsubstituted dimethylamide and -33 for N-methyl-substituted dimethylamide.The N,N-dimethylamides are particularly suitable for the investigation of the rates and mechanisms of intramolecular electron-transfer processes by picosecond and nanosecond pulse techniques.

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