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194918-33-7

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194918-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 194918-33-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,9,1 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 194918-33:
(8*1)+(7*9)+(6*4)+(5*9)+(4*1)+(3*8)+(2*3)+(1*3)=177
177 % 10 = 7
So 194918-33-7 is a valid CAS Registry Number.

194918-33-7SDS

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 1,3,3-trimethylindoline carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:194918-33-7 SDS

194918-33-7Downstream Products

194918-33-7Relevant articles and documents

Reaction of spironaphthoxazine with acid

Nishikiori, Hiromasa,Shimamura, Suguru,Fujii, Tsuneo

, p. 100 - 106 (2013)

The reaction of spironaphthoxazine (SNO) with acid in ethanol was investigated by spectroscopic analyses SNO was protonated and then transformed into a complex in an acidic ethanol solution in the dark. It is presumed that the complex contains a hydrated proton and its structure is similar to that of the metal complex of a merocyanine-type isomer photoderived from SNO based on its UV-vis absorption and fluorescence spectra. The complex dissociated into SNO by adding base. The complex was further changed under acidic conditions after a long time. Highly concentrated acid decomposed SNO to an indoline compound having a carboxyl group and 1-amino-2-naphthol, which was revealed by fluorescence, IR, and GC-MS analyses. These reaction processes were promoted by UV irradiation.

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