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N-(2-hydrazinyl-2-oxoethyl)-3,4,5-trimethoxybenzamide (non-preferred name) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63203-45-2

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63203-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63203-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,0 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63203-45:
(7*6)+(6*3)+(5*2)+(4*0)+(3*3)+(2*4)+(1*5)=92
92 % 10 = 2
So 63203-45-2 is a valid CAS Registry Number.

63203-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-hydrazinyl-2-oxoethyl)-3,4,5-trimethoxybenzamide

1.2 Other means of identification

Product number -
Other names N-(2-hydrazino-2-oxoethyl)-3,4,5-trimethoxybenzamide

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:63203-45-2 SDS

63203-45-2Relevant academic research and scientific papers

COMPOUNDS FOR THE TREATMENT OF PARAMOXYVIRUS VIRAL INFECTIONS

-

Paragraph 0358, (2014/03/25)

Disclosed herein are new antiviral compounds, together with pharmaceutical compositions that include one or more antiviral compounds, and methods of synthesizing the same. Also disclosed herein are methods of ameliorating and/or treating a paramyxovirus viral infection with one or more small molecule compounds. Examples of paramyxovirus infection include an infection caused by human respiratory syncytial virus (RSV).

Novel heterobivalent tacrine derivatives as cholinesterase inhibitors with notable selectivity toward butyrylcholinesterase

Elsinghorst, Paul W.,González Tanarro, Camino M.,Gütschow, Michael

, p. 7540 - 7544 (2007/10/03)

Two series of novel heterobivalent tacrine derivatives were synthesized. A trimethoxy substituted benzene was linked to the tacrine moiety by a hydrazide-based linker. The compounds were evaluated as cholinesterase inhibitors, and trimethoxybenzoic acid derivatives with 11- or 12-atom spacers were the most potent inhibitors of human acetylcholinesterase. The inhibitors showed a surprising selectivity toward human butyrylcholinesterase, where several trimethoxyphenylpropionic acid derivatives had IC50 values less than 250 pM.

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