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5,6-dihydro-4H-[1,3]thiazolo[5,4,3-ij]quinolin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68729-18-0

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68729-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68729-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,7,2 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 68729-18:
(7*6)+(6*8)+(5*7)+(4*2)+(3*9)+(2*1)+(1*8)=170
170 % 10 = 0
So 68729-18-0 is a valid CAS Registry Number.

68729-18-0SDS

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 AC1L3OXU

1.2 Other means of identification

Product number -
Other names 2-Oxo-5,6-dihydro-4H-thiazolo<5,4,3-ij>-chinolin

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:68729-18-0 SDS

68729-18-0Downstream Products

68729-18-0Relevant academic research and scientific papers

Nucleic acid binding dyes and uses therefor

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Page/Page column 29, (2015/12/25)

The invention provides novel compounds and compositions of Formulas I and II, as well as methods of using them. The compounds can be used, for example, to quantify an amount of double stranded DNA in a sample subjected to nucleic acid amplification, or fo

NUCLEIC ACID BINDING DYES AND USES THEREFOR

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, (2010/09/18)

The invention provides novel compounds and compositions of Formulas I and II, as well as methods of using them. The compounds can be used, for example, to quantify an amount of double stranded DNA in a sample subjected to nucleic acid amplification, or fo

Process for the manufacture of 2(3H)-benzothiazolones substituted in 3-position

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, (2008/06/13)

A process for the manufacture of a 2(3H)-benzothiazolone compound substituted in 3-position, or of a 2(3H)-naphthothiazolone compound substituted in 3-position which comprises treating a 2(3H)-iminobenzothiazoline compound substituted in 3-position or a 2

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