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benzyl 1-(N,N-dibenzylamino)cyclopropanecarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119326-95-3

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119326-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119326-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,3,2 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 119326-95:
(8*1)+(7*1)+(6*9)+(5*3)+(4*2)+(3*6)+(2*9)+(1*5)=133
133 % 10 = 3
So 119326-95-3 is a valid CAS Registry Number.

119326-95-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 1-(N,N-dibenzylamino)cyclopropanecarboxylate

1.2 Other means of identification

Product number -
Other names benzyl 1-(dibenzylamino)cyclopropanecarboxylate

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:119326-95-3 SDS

119326-95-3Relevant academic research and scientific papers

MK2 INHIBITORS AND USES THEREOF

-

Paragraph 00645, (2014/10/03)

The present invention provides compounds, compositions thereof, and methods of using the same.

Decarboxylation of 1-Aminocyclopropanecarboxylic Acid and Its Derivatives

Vaidyanathan, Ganesan,Wilson, Joseph W.

, p. 1810 - 1815 (2007/10/02)

The question of whether the title compounds could be decarboxylated to cyclopropanone derivatives was answered in the affirmative by the following observations. (1) Compound 11a was decarboxylated by 1,2,3-indantrione in acetonitrile, benzene, or methanol.The initially formed intermediate could be trapped by N-phenylmaleimide (to form 3), by diethyl azodicarboxylate (to form an unstable adduct), by ninhydrin itself (to form 5) or by a proton (in methanol, to form 8). (2) Compound 11d was decarboxylated by phenylbis(trifluoroacetato-O)iodine to yield carbinolamine 12d.cis-2,3-Dideuterio-11d yielded cis-2,3-dideuterio-12d under the same conditions. (3) ACC was decarboxylated by phenanthroquinone to yield oxazole 9, probably by way of oxazoline 10.

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