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Glycine, N-(3,4,5-trimethoxybenzoyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92502-39-1 Structure
  • Basic information

    1. Product Name: Glycine, N-(3,4,5-trimethoxybenzoyl)-, ethyl ester
    2. Synonyms: N-(3,4,5-Trimethoxy-benzoyl)-glycin-aethylester;N-(3,4,5-trimethoxy-benzoyl)-glycine ethyl ester;N-<3.4.5-Trimethoxy-benzoyl>-glycin-aethylester;(3.4.5-Trimethoxy-benzamino)-essigsaeure-aethylester;N-Galloylglycinaethylester;(3,4,5-Trimethoxy-benzoylamino)-acetic acid ethyl ester;
    3. CAS NO:92502-39-1
    4. Molecular Formula: C14H19NO6
    5. Molecular Weight: 297.308
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92502-39-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Glycine, N-(3,4,5-trimethoxybenzoyl)-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Glycine, N-(3,4,5-trimethoxybenzoyl)-, ethyl ester(92502-39-1)
    11. EPA Substance Registry System: Glycine, N-(3,4,5-trimethoxybenzoyl)-, ethyl ester(92502-39-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 92502-39-1(Hazardous Substances Data)

92502-39-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92502-39-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,0 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92502-39:
(7*9)+(6*2)+(5*5)+(4*0)+(3*2)+(2*3)+(1*9)=121
121 % 10 = 1
So 92502-39-1 is a valid CAS Registry Number.

92502-39-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl ((3,4,5-trimethoxybenzoyl)amino)acetate

1.2 Other means of identification

Product number -
Other names N-(3,4,5-trimethoxy-benzoyl)-glycine ethyl ester

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:92502-39-1 SDS

92502-39-1Relevant articles and documents

Copper-Catalyzed Aerobic Oxidative [2 + 3] Cyclization/Aromatization Cascade Reaction: Atom-Economical Access to Tetrasubstituted 4,5-Biscarbonyl Imidazoles

Xie, Jialin,Huang, Yuanqiong,Song, Hongjian,Liu, Yuxiu,Wang, Qingmin

supporting information, p. 6056 - 6059 (2017/11/27)

An atom-economical method for accessing tetrasubstituted 4,5-biscarbonylimidazoles by reaction between glycine derivatives and 5-alkoxyoxazoles is reported. The method, which involves a copper-catalyzed aerobic oxidative [2 + 3] cyclization/aromatization

COMPOUNDS FOR THE TREATMENT OF PARAMOXYVIRUS VIRAL INFECTIONS

-

Paragraph 0357, (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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