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α-[(Dimethylamino)methyl]benzyl=benzoate is a complex organic chemical compound with the molecular formula C17H19NO2. It is a derivative of benzoic acid, featuring a dimethylaminomethyl group attached to the benzyl moiety. α-[(Dimethylamino)methyl]benzyl=benzoate is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain drugs and pesticides. Its structure provides a unique combination of aromatic and aliphatic characteristics, which can influence its reactivity and physical properties. The compound's name reflects its structure, indicating the presence of a dimethylamino group on a methylene bridge that connects to a benzyl group, which in turn is esterified with benzoic acid.

25314-75-4

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25314-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25314-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,1 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25314-75:
(7*2)+(6*5)+(5*3)+(4*1)+(3*4)+(2*7)+(1*5)=94
94 % 10 = 4
So 25314-75-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H19NO2/c1-18(2)13-16(14-9-5-3-6-10-14)20-17(19)15-11-7-4-8-12-15/h3-12,16H,13H2,1-2H3

25314-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(dimethylamino)-1-phenylethyl] benzoate

1.2 Other means of identification

Product number -
Other names Benzoesaeure-(2-dimethylamino-1-phenyl-aethylester)

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:25314-75-4 SDS

25314-75-4Downstream Products

25314-75-4Relevant academic research and scientific papers

Novel Zinc-Promoted Alkylation of Iminium Salts. New Synthesis of Benzylisoquinoline, Phthalidylisoquinoline, and Protoberberine Alkaloids and Related Compounds

Shono, Tatsuya,Hamaguchi, Hiroshi,Sasaki, Manji,Fujita, Shumei,Nagami, Kimihiko

, p. 1621 - 1628 (2007/10/02)

Zinc-promoted reductive coupling reaction of iminium salts with alkyl halides was found to be a successful key reaction for synthesis of a variety of alkaloids such as benzylisoquinoline, phthalidylisoquinoline, and protoberberine alkaloids.More specifically, laudanosine, cordrastine, hydrastine, narcotine, tetrahydropalmatine, and canadine were obtained.A new route for the synthesis of the emetine and yohimbine skeletons was exploited.

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