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17112-82-2

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17112-82-2 Usage

General Description

1-NAPHTHALENEMETHYL ISOTHIOCYANATE is a chemical compound derived from naphthalene and used as a reagent in organic synthesis. It is a yellow to orange liquid with a strong, pungent odor. 1-NAPHTHALENEMETHYL ISOTHIOCYANATE is primarily used in the production of pharmaceuticals, agrochemicals, and dyes. It is also a potent irritant and sensitizer, and exposure to this chemical can cause skin and eye irritation, respiratory problems, and allergic reactions. Additionally, it is considered to be a potential carcinogen and mutagen, and therefore, proper handling and safety precautions are necessary when working with 1-NAPHTHALENEMETHYL ISOTHIOCYANATE.

Check Digit Verification of cas no

The CAS Registry Mumber 17112-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,1 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17112-82:
(7*1)+(6*7)+(5*1)+(4*1)+(3*2)+(2*8)+(1*2)=82
82 % 10 = 2
So 17112-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NS/c14-9-13-8-11-6-3-5-10-4-1-2-7-12(10)11/h1-7H,8H2

17112-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Naphthalenemethyl isothiocyanate

1.2 Other means of identification

Product number -
Other names 1-(isothiocyanatomethyl)naphthalene

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:17112-82-2 SDS

17112-82-2Relevant articles and documents

Colorimetric Naphthalene-Based Thiosemicarbazide Anion Chemosensors with an Internal Charge Transfer Mechanism

Farrugia, Kristina N.,Makuc, Damjan,Podborska, Agnieszka,Szaci?owski, Konrad,Plavec, Janez,Magri, David C.

, p. 4415 - 4422 (2016)

A series of thiosemicarbazide anion chemosensors substituted with naphthalene and 4-nitrophenyl or phenyl units were synthesized. The molecules were characterized by using1H,13C DEPT and15N NMR spectroscopy. The anion bind

ISOTHIOCYNATES AND GLUCOSINOLATE COMPOUNDS AND ANTI-TUMOR COMPOSITIONS CONTAINING SAME

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Paragraph 0094; 0096; 0111, (2013/05/21)

The present invention provides glucosinolate and isothiocyanate compounds and related methods for synthesizing these compounds and analogs. In certain embodiments, these glucosinolate and isothiocyanate compounds are useful and chemopreventive and or chemotherapeutic agents.

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