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17273-44-8

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17273-44-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17273-44-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,7 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17273-44:
(7*1)+(6*7)+(5*2)+(4*7)+(3*3)+(2*4)+(1*4)=108
108 % 10 = 8
So 17273-44-8 is a valid CAS Registry Number.

17273-44-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name α-naphthoic acid, sodium salt

1.2 Other means of identification

Product number -
Other names Na-Naphthalincarbonat-(1)

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:17273-44-8 SDS

17273-44-8Upstream product

17273-44-8Relevant articles and documents

1-butyl-3-methylimidazole naphthoic formate ionic liquid and preparation method and application thereof

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Paragraph 0056, (2016/10/17)

The invention discloses 1-butyl-3-methylimidazole naphthoic formate ionic liquid and a preparation method and application thereof. The structural formula of the 1-butyl-3-methylimidazole naphthoic formate ionic liquid is shown in the formula (I). The preparation method of the 1-butyl-3-methylimidazole naphthoic formate ionic liquid comprises the steps that 1, 1-naphthoic acid is added into an excessive amount of a sodium hydroxide solution to be subjected to a reaction to obtain reaction liquid A; 2, chloro1-butyl-3-methylimidazole is added into the reaction liquid A to be subjected to a reaction to obtain reaction liquid B; 3, water in the reaction liquid B is removed, then absolute ethyl alcohol is added, freezing crystallization and filtering are performed to remove NaCl in the system, and then ethyl alcohol is removed to obtain the 1-butyl-3-methylimidazole naphthoic formate ionic liquid. The 1-butyl-3-methylimidazole naphthoic formate ionic liquid has more conjugation structures compared with conventional ionic liquid, the fluorescent effect is better, and the sensitivity in fluorescence detection is greatly improved; the 1-butyl-3-methylimidazole naphthoic formate ionic liquid is hydrophobic ionic liquid, the stronger fluorescent sensitivity enhancing effect is achieved for weak fluorescent pollutant, and the higher application value is achieved on compound trace chromatography and fluorescence analysis.

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