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1-Propanone, 2,2-dimethoxy-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38868-78-9

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38868-78-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38868-78-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,6 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38868-78:
(7*3)+(6*8)+(5*8)+(4*6)+(3*8)+(2*7)+(1*8)=179
179 % 10 = 9
So 38868-78-9 is a valid CAS Registry Number.

38868-78-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethoxy-1-phenylpropan-1-one

1.2 Other means of identification

Product number -
Other names 2,2-dimethoxypropiophenone

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:38868-78-9 SDS

38868-78-9Relevant academic research and scientific papers

Rapid, One-Step Synthesis of α-Ketoacetals via Electrophilic Etherification

Paris, Timothy J.,Schwartz, Chris,Sundall, Eric,Willand-Charnley, Rachel

, p. 14797 - 14811 (2021/10/20)

Herein, we report a rapid, one-step synthesis of α-ketoacetals via electrophilic etherification of α-alkoxy enolates and monoperoxyacetals. Methyl, primary, and secondary α-ketoacetals were obtained in 44-63% yields from tetrahydropyranyl substrates; usin

New platinum-catalysed dihydroalkoxylation of allenes

Munoz, Maria Paz,De La Torre, Maria C.,Sierra, Miguel A.

supporting information; experimental part, p. 2189 - 2194 (2010/11/04)

A new platinum-catalysed dihydroalkoxylation of alienes is described to give aliphatic acetals by an unexpected attack of two molecules of methanol to the terminal carbon of the aliene moiety. Deuteration experiments suggest an unprecedented formal 1,3-dipolar addition of methanol to a zwitterionic platinum carbene as the key step. The first platinum-catalysed intermolecular carbonbased nucleophile addition to alienes is also reported.

Solvent directed electrophilic iodination and phenylselenenylation of activated alkyl aryl ketones

Panunzi, Barbara,Rotiroti, Lucia,Tingoli, Marco

, p. 8753 - 8756 (2007/10/03)

A mixture of molecular iodine and phenyliodine(III) bis(trifluoroacetate) (BTI) in CH3CN (or CH3OH) iodinates the aromatic ring of some activated alkyl aryl ketones. A different outcome results if PhSeSePh is used instead of I2

Substituted benzyl oximino compounds

-

, (2008/06/13)

The present invention relates to benzyloxyimino compounds of the formula I, where: R1to R4, X, Y, and Z are as defined in the specification.

Regiospecific synthesis of α-diones, α,α-dialkoxyketones and α-alkoxy-α-sulfenylated ketones

Tehrani,Boeykens,Tyvorskii,Kulinkovich,De Kimpe

, p. 6541 - 6548 (2007/10/03)

A convenient synthesis of α-diones and their monoprotected acetals, i.e. α-ketoacetals, was developed by mercury induced solvolysis of regiospecifically formed α-chloro-α-(alkylthio)ketones. Analogously, α-alkoxy-α-sulfenylated ketones were formed when reacting α-chloro-α-sulfenylated ketones with an alkaline alcoholic medium, α-Alkoxy-α-sulfenylated ketones themselves could be transformed into α-diones or ?-ketoacetals, which in turn were hydrolyzed under anhydrous conditions into the corresponding α-diones. (C) 2000 Elsevier Science Ltd.

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 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.

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.

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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