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(8-carboxynaphthalen-1-yl)mercury is a chemical compound that consists of a mercury atom bound to a naphthalene ring with a carboxylic acid group attached to the naphthalene ring. It is a potentially toxic and hazardous substance that is primarily used in research and chemical synthesis.

6314-27-8

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6314-27-8 Usage

Uses

Used in Pharmaceutical Research:
(8-carboxynaphthalen-1-yl)mercury is used as a research compound for studying its properties and potential applications in the development of pharmaceuticals.
Used in Organic Chemistry:
(8-carboxynaphthalen-1-yl)mercury is used as a reagent in organic synthesis for the preparation of various organic compounds.
Used in Chemical Synthesis:
(8-carboxynaphthalen-1-yl)mercury is used as a chemical intermediate in the synthesis of other complex organic molecules.
It is important to use caution and proper safety measures when working with or handling (8-carboxynaphthalen-1-yl)mercury to minimize the potential risks associated with its use, as it poses significant environmental and health risks, especially if mishandled or improperly disposed of.

Check Digit Verification of cas no

The CAS Registry Mumber 6314-27-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6314-27:
(6*6)+(5*3)+(4*1)+(3*4)+(2*2)+(1*7)=78
78 % 10 = 8
So 6314-27-8 is a valid CAS Registry Number.

6314-27-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name anhydro-2-p-Tolyl-3-phenyl-5-mercapto-1,3,4-thiadiazoliumhydroxid

1.2 Other means of identification

Product number -
Other names anhydro-8-hydroxymercuric-1-naphthoic acid

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:6314-27-8 SDS

6314-27-8Relevant academic research and scientific papers

Synthesis and photophysical properties of a porphyrin-perinaphthothioindigo dye

Ogawa, Kazuya,Dy, Joanne,Maeda, Rena,Nagatsuka, Yasunori,Kamada, Kenji,Kobuke, Yoshiaki

, p. 821 - 830 (2013/09/24)

A new porphyrin-perinaphthothioindigo composite, where porphyrin and perinaphthothioindigo dye are connected though a triple bond, was synthesized. In UV-vis absorption spectra of the composite, absorption originating from the trans-isomer appeared at 655

THIAZOLE DERIVATIVES AS SGLT2 INHIBITORS AND PHARMACEUTICAL COMPOSITION COMPRISING SAME

-

, (2012/01/06)

The present invention relates to a novel compound with thiazole ring having an inhibitory activity against sodium-dependent glucose cotransporter 2 (SGLT2) being present in the intestine and kidney, and a pharmaceutical composition comprising the same as an active ingredient, which is useful for preventing or treating metabolic disorders, particularly diabetes.

Porphyrin compound, process for producing porphyrin compound, three-dimensional optical recording material, and three-dimensional optical recording medium

-

Page/Page column 25, (2010/11/28)

Compounds that are suitable to be used for three-dimensional optical recording materials, etc. The compounds each have a structure that allows pi-electron conjugation to be achieved by linking a porphyrin ring and a perinaphthothioindigo ring to each other with a straight-chain atomic group. The compounds of the present invention are suitable to be used for three-dimensional optical recording materials, etc. since they have a high two-photon absorption efficiency and undergo photochromism effectively through optical absorption.

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