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Ethyl 3-methoxy-4-nitrobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10259-23-1

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10259-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10259-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,5 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10259-23:
(7*1)+(6*0)+(5*2)+(4*5)+(3*9)+(2*2)+(1*3)=71
71 % 10 = 1
So 10259-23-1 is a valid CAS Registry Number.

10259-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 3-methoxy-4-nitrobenzoate

1.2 Other means of identification

Product number -
Other names 3-Methoxy-4-nitro-benzoesaeure-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:10259-23-1 SDS

10259-23-1Relevant academic research and scientific papers

COMPOUNDS FOR THE TREATMENT OF PARAMOXYVIRUS VIRAL INFECTIONS

-

Paragraph 0552, (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).

Synthesis of symmetric diester-functionalised Troeger's base analogues

Bhuiyan, M. Delower H.,Zhu, Kai-Xian,Jensen, Paul,Try, Andrew C.

supporting information; experimental part, p. 4662 - 4670 (2010/10/19)

The yields of ester-functionalised Troeger's base analogues are dramatically improved by incorporating an electron-donating group on the aromatic ring and/or enhancing solubil- ity of the aniline unit. In addition to 2,8-diester compounds, 1,7-, 3,9- and 4,10-diester-functionalised Troeger's base analogues have been prepared for the first time.

Synthesis of Benzothiazoles. α-Amino-(4-hydroxy-6-benzothiazolyl)propionic Acid.

Ismail, Ibrahim A.,Sharp, Dale E.,Chedekel, Miles R.

, p. 2243 - 2246 (2007/10/02)

The tentative structure assigned to the photobiologically important skin pigment pheomelanin is based on degradative studies of the natural chromophore.The title compound was reported to be one of several key amino acids isolated in these studies.The identity of this benzothiazole derivative has now been confirmed via an unambiguous eight-step total synthesis starting from 5-methyl-2-nitrophenol.

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