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17268-47-2

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17268-47-2 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 52, p. 5266, 1987 DOI: 10.1021/jo00232a038

Check Digit Verification of cas no

The CAS Registry Mumber 17268-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,6 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17268-47:
(7*1)+(6*7)+(5*2)+(4*6)+(3*8)+(2*4)+(1*7)=122
122 % 10 = 2
So 17268-47-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H16N2O/c1-8(2)6-5-7(10)9(3)4/h5-6H2,1-4H3

17268-47-2SDS

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 3-(dimethylamino)-N,N-dimethylpropanamide

1.2 Other means of identification

Product number -
Other names Propanamide,3-(dimethylamino)-N,N-dimethyl

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:17268-47-2 SDS

17268-47-2Relevant articles and documents

A 'magic bridge': effect of methylene chain length on the photochemistry of radical cations produced from bifunctional X-(CH2)n-Y molecules

Nuzhdin, Kirill B.,Kobzarenko, Aleksei V.,Barabanov, Igor I.,Feldman, Vladimir I.

, p. 268 - 269 (2009)

The radical cations of aminoamides Me2N(CH2)nC(O)NMe2 and aminoethers Me2N(CH2)nOMe reveal selective photoinduced intramolecular H transfer from methylene bridge at a specific ch

METHOD FOR PRODUCING ALPHA, BETA-UNSATURATED CARBOXYLIC ACID-N,N-DISUBSTITUTED AMIDE AND METHOD FOR PRODUCING 3-ALKOXYCARBOXYLIC ACID-N,N-DISUBSTITUTED AMIDE

-

Page/Page column 19; 20, (2012/03/26)

The invention is directed to a technique for effectively producing an amide compound suitable for use as a solvent or a detergent on a large scale and at low cost.

Tandem conjugate addition-aldol reaction to α,β-unsaturated esters and ketones using titanium amide

Hosomi, Akira,Yanagi, Toshiharu,Hojo, Makoto

, p. 2371 - 2374 (2007/10/02)

Titanium dialkylamide, readily available, adds to a α,β-unsaturated esters and ketones in a conjugate addition mode to give ester and ketone enolates, respectively, which are successively quenched with electrophiles such as aldehydes and acetals. The aldol products can be readily converted to the corresponding deaminated or dehydrated derivatives selectively.

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