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Ethanone, 2,2-bis(1-methylethoxy)-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21983-73-3

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21983-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21983-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,8 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21983-73:
(7*2)+(6*1)+(5*9)+(4*8)+(3*3)+(2*7)+(1*3)=123
123 % 10 = 3
So 21983-73-3 is a valid CAS Registry Number.

21983-73-3SDS

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 1-phenyl-2,2-di(propan-2-yloxy)ethanone

1.2 Other means of identification

Product number -
Other names 2,2-Diisopropoxy-1-phenylethanone

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:21983-73-3 SDS

21983-73-3Downstream Products

21983-73-3Relevant academic research and scientific papers

YCL3-catalyzed highly selective conversion of arylglyoxal to α-aryl- α-hydroxyacetic ester: Dramatic influence of base

Likhar, Pravin R.,Bandyopadhyay, Ananda K.

, p. 538 - 540 (2007/10/03)

Yttrium chloride catalyzed reaction of arylglyoxal and alcohol resulted in highly selective formation of α-aryl-α-hydroxyacetic ester under the influence of an added base (triethylamine, pyridine, piperidine) and afforded acetal in the absence of the base. The possible role of the additive (base) is discussed.

Liquid photoinitiator mixtures

-

, (2008/06/13)

Liquid highly active photoinitiators are obtained by dissolving a solid photoinitiator of the titanocene type in liquid photoinitiators of the acetal or ketal type. The liquid mixtures have a long dark storage stability.

Oxygen-containing titanocenes, and the use thereof

-

, (2008/06/13)

Titanocenes of the formula I STR1 in which R1 are cyclopentadienyl? groups and R2 and R3 are aromatic radicals which are substituted in both ortho-positions by fluorine and, in addition, are substituted by an acyloxy group are suitable as photoinitiators for the photopolymerization of ethylenically unsaturated compounds.

Titanocenes, the use thereof, and N-substituted pyrroles

-

, (2008/06/13)

Titanocenes containing two 5-membered cyclodienyl groups, for example cyclopentadienyl, and one or two 6-membered carbocyclic or 5- or 6-membered heterocyclic aromatic rings which are substituted by a fluorine atom in at least one of the two ortho-positions to the titanium-carbon bond and contain, as a further substituent, unsubstituted or substituted 1-pyrryl, are suitable as photoinitiators for radiation-induced polymerization of ethylenically unsaturated compounds.

Titanocenes, the use thereof, and n-substituted fluoroanilines

-

, (2008/06/13)

Titanocenes containing two 5-membered cyclodienyl gropus, for example cyclopentadienyl, and one or two 6-membered carbocyclic or 5- or 6-membered heterocyclic aromatic rings which are substituted by a fluorine atom in at least one of the two ortho-positions to the titanium-carbon bond and contain, as further substituents, a substituted amino radical, are suitable as photoinitiators for radiation-induced polymerization of ethylenically unsaturated compounds.

Novel nitrogen-containing titanocenes, and the use thereof

-

, (2008/06/13)

Titanocenes of the formula I STR1 in which R1 are cyclopentadienyl? groups and R2 and R3 are aromatic radicals which are substituted in both ortho-positions by fluorine and, in addition, are substituted by a pyrrylalkyl group, amidoalkyl group or imidoalkyl group, are suitable as photoinitiators for the photopolymerization of ethylenically unsaturated compounds.

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