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27908-75-4

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27908-75-4 Usage

Preparation

2-Methylquinoline and 4,5,6,7-Tetrachloroisobenzofuran-1,3-dione condensation.

Properties and Applications

brilliant green yellow. Standard Light Fastness Heat-resistant(℃) water Sodium Carbonate(5%) Hydrochloric acid(5%) Melting point Stable ISO Good >300 280 Insoluble Well Well

Standard

Light Fastness

Melting point

Stable

ISO

Good

Check Digit Verification of cas no

The CAS Registry Mumber 27908-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,0 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27908-75:
(7*2)+(6*7)+(5*9)+(4*0)+(3*8)+(2*7)+(1*5)=144
144 % 10 = 4
So 27908-75-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H7Cl4NO2/c19-13-11-12(14(20)16(22)15(13)21)18(25)10(17(11)24)9-6-5-7-3-1-2-4-8(7)23-9/h1-6,10H

27908-75-4SDS

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 4,5,6,7-Tetrachloro-2-(2-quinolinyl)-1H-indene-1,3(2H)-dione

1.2 Other means of identification

Product number -
Other names 1H-Isoindol-1-one,4,5,6,7-tetrachloro-2,3-dihydro

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:27908-75-4 SDS

27908-75-4Downstream Products

27908-75-4Relevant articles and documents

PHENANTHROLINE COMPOUND AND COLORANT

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Paragraph 0068-0069; 0075-0076, (2017/08/02)

PROBLEM TO BE SOLVED: To provide a phenanthroline compound having a new skeleton available as a yellow pigment. SOLUTION: The phenanthroline compound is represented by the general formula in the figure. (In the general formula (1), R1 and R2 each independently represent a hydrogen atom, or an optionally substituted alkyl group, aryl group or indandione group, provided that at least one of R1 and R2 is the optionally substituted indandione group; and R3 and R4 each independently represent a hydrogen atom or a phenyl group.) SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

Pigment dispersing agent, pigment composition and pigment dispersion

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Page/Page column 17-18, (2008/06/13)

A pigment dispersing agent wherein a quinophthalone structure is bonded to a triazine structure through an arylene group or a heteroaromatic ring and a basic functional group is bonded to triazine ring through a connecting group which pigment dispersing a

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