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ETHYL 3-(N-BENZYL-N-METHYLAMINO)PROPANOATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25772-94-5

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25772-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25772-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,7,7 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25772-94:
(7*2)+(6*5)+(5*7)+(4*7)+(3*2)+(2*9)+(1*4)=135
135 % 10 = 5
So 25772-94-5 is a valid CAS Registry Number.

25772-94-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-[benzyl(methyl)amino]propanoate

1.2 Other means of identification

Product number -
Other names ETHYL 3-(N-BENZYL-N-METHYLAMINO)PROPANOATE

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:25772-94-5 SDS

25772-94-5Relevant academic research and scientific papers

DIAZEPINONE DERIVATIVES AND THEIR USE IN THE TREATMENT OF HEPATITIS B INFECTIONS

-

Page/Page column 135-136, (2018/02/28)

Provided herein are compounds of formula (I) and (V) useful for the treatment of HBV infection in a subject in need thereof, pharmaceutical compositions thereof, and methods of inhibiting, suppressing, or preventing HBV infection in the subject.

Samarium(III) triflate catalyzed conjugate addition of amines to electron-deficient alkenes

Yadav,Ramesh Reddy,Gopal Rao,Narsaiah,Subba Reddy

, p. 3447 - 3450 (2008/09/19)

Amines undergo smooth nucleophilic addition to α,β-unsaturated compounds in the presence of a catalytic amount of samarium(III) triflate at ambient temperature to produce the corresponding β-amino compounds in excellent yields. This method is simple, convenient, and works efficiently under mild conditions. Georg Thieme Verlag Stuttgart.

Potent, orally active corticotropin-releasing factor receptor-1 antagonists containing a tricyclic pyrrolopyridine or pyrazolopyridine core

Dyck, Brian,Grigoriadis, Dimitri E.,Gross, Raymond S.,Guo, Zhiqiang,Haddach, Mustapha,Marinkovic, Dragan,McCarthy, James R.,Moorjani, Manisha,Regan, Collin F.,Saunders, John,Schwaebe, Michael K.,Szabo, Tomas,Williams, John P.,Zhang, Xiaohu,Bozigian, Haig,Chen, Ta Rung

, p. 4100 - 4110 (2007/10/03)

Two new classes of tricyclic-based corticotropin-releasing factor (CRF 1) receptor-1 antagonists were designed by constraining known 1H-pyrrolo[2,3-b]pyridine and 1H-pyrazolo[3,4-b]pyridine ligands. Pyrrole- and pyrazole-based molecules 19g and

Methods and compounds for treating depression and other disorders

-

, (2008/06/13)

The present invention features compounds active at both the serotonin reuptake site and the N-methyl-D-aspartate (NMDA) receptor and the use of such compounds for treating different disorders. Compounds having activity at the serotonin reuptake site and the NMDA receptor (“multi-active compounds”) can be used to treat different types of disorders such as depression, obsessive-compulsive disorders (OCD), sleep, disorders, sexual dysfunction, and eating disorders. Preferably, the multi-active compounds are used to treat depression.

Compounds active at a novel site on receptor-operated calcium channels useful for treatment of neurological disorders and diseases

-

, (2008/06/13)

Method and compositions for treating a patient having a neurological disease or disorder, such as stroke, head trauma, spinal cord injury, spinal cord ischemia, ischemia- or hypoxia-induced nerve cell damage, epilepsy, anxiety, neuropsychiatric or cogniti

Cerium(IV) oxidations of β-aminoketones, VIII: Synthesis of 1,2,3,4-tetrahydroisoquinolines with differently substituted piperidine parts

Holzgrabe,Inkman

, p. 209 - 215 (2007/10/02)

1- and 3-Alkyl- and/or aryl substituted tetrahydroisoquinolines are obtained by oxidative cyclisation of N-benzyl-β-aminoketones with cerium(IV) sulphate. In nearly all cases formation of mixtures of diastereomeres is observed. If the ketone function is r

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