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1-Propanone, 1-[4-[(2-hydroxyethyl)thio]phenyl]-2-methyl-2-(4-morpholinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88324-58-7

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88324-58-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88324-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,2 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88324-58:
(7*8)+(6*8)+(5*3)+(4*2)+(3*4)+(2*5)+(1*8)=157
157 % 10 = 7
So 88324-58-7 is a valid CAS Registry Number.

88324-58-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-(2-hydroxyethylthio)-phenyl]-2-methyl-2-morpholin-4-yl-propan-1-one

1.2 Other means of identification

Product number -
Other names 1-[4-(2-hydroxyethylthio)-phenyl]-2-methyl-2-morpholino-propan-1-one

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:88324-58-7 SDS

88324-58-7Downstream Products

88324-58-7Relevant academic research and scientific papers

New compound, the compound of the formula, newcompound and radiation-sensitive composition containing a thermosetting film

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Paragraph 0108; 0109; 0112, (2016/12/16)

PROBLEM TO BE SOLVED: To provide a novel compound having low sublimability and exhibiting high radiation sensitivity on use as a photopolymerization initiator, a method for producing the novel compound, and a radiation-sensitive composition including the

NOVEL PHOTOINITIATORS AND THEIR APPLICATIONS

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Page/Page column 19, (2010/11/24)

Photoinitiators of formula (Ia) or (Ib) having chain transfer groups, wherein n is 1 or 2; PI is for example a group of formula (IIa); PI' inter alia is a group of formula (IIIa); Ar is for example phenyl; Ar2 is inter alia phenylene; R1 and R2 are for ex

Novel morpholinoketone derivatives, and preparation process and uses of the same

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Page 6, (2010/02/06)

Disclosed herein are novel morpholinoketone derivatives of formula (I): wherein each of the substituents is given the definition as set forth in the Specification and claims. Also disclosed are the preparation process of the derivatives, and their uses as a photoinitiator in photopolymerizable compositions.

Novel morpholinoketone derivatives, and preparation process and uses of the same

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Page 6, (2010/11/30)

Disclosed herein are novel morpholinoketone derivatives of formula (I): wherein each of the substituents is given the definition as set forth in the Specification and claims. Also disclosed are the preparation process of the derivatives, and their uses as

Novel aminoketone derivatives and preparation process and uses of the same as photoinitiators

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, (2008/06/13)

Disclosed herein are novel morpholinoketone derivatives of formula (I): wherein each of the substituents is given the definition as set forth in the Specification and Claims.Also disclosed are the preparation process of the derivatives, and their uses as a photoinitiator in photopolymerizable compositions.

Aminoaryl ketone photoinitiators

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, (2008/06/13)

The photopolymerizable mixture described contains (A) at least one ethylenically unsaturated photopolymerisable compound, (B) a photoinitiator of the formula I STR1 and (C) a photosensitiser from the group of aromatic carbonyl compounds having a triplet energy of 225-310 kJ/mol, for example xanthones, thioxianthones, coumarins, phthalimides, phenones and the like. Ar is phenyl substituted in the 4-position by a substituted amino group, R1 and R2 are alkyl, R3 and R4 are alkyl or alkoxyalkyl, or R3 and R4 together are 3-oxapentamethylene. Said sensitisers (C) raise the activity of said photoinitiators (B) without shortening the shelf life of the mixtures. The photocurable mixtures are used especially as binders for printing inks or paints.

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