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Methyl 4-(5-methoxy-2-nitrophenyl)-3-oxobutyrate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

130916-41-5

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130916-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130916-41-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,9,1 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 130916-41:
(8*1)+(7*3)+(6*0)+(5*9)+(4*1)+(3*6)+(2*4)+(1*1)=105
105 % 10 = 5
So 130916-41-5 is a valid CAS Registry Number.

130916-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 4-(5-methoxy-2-nitrophenyl)-3-oxobutyrate

1.2 Other means of identification

Product number -
Other names -

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:130916-41-5 SDS

130916-41-5Relevant academic research and scientific papers

TRIAZOLOBENZAZEPINES AS VASOPRESSIN V1A RECEPTOR ANTAGONISTS

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Page/Page column 102, (2019/07/19)

The present invention relates to 5,6-dihydro-4H-[1,2,4]triazolo[4,3-a][1]benzazepine derivatives of general formula (I) and/or salts thereof and/or geometric isomers thereof and/or stereoisomers thereof and/or enantiomers thereof and/or racemates thereof and/or diastereomers thereof and/or biologically active metabolites thereof and/or prodrugs thereof and/or solvates thereof and/or hydrates thereof and/or polymorphs thereof which are centrally and/or peripherally acting V1a receptor modulators, particularly V1a receptor antagonists. Additional subject of the present invention is the process for the preparation of the compounds and the intermediates of the preparation process as well. The invention also relates to the pharmaceutical compositions containing the compounds or together with one or more other active substances, as well as to the use in the treatment and/or prophylaxis of a disease or condition associated with V1a receptor function.

Synthesis of 6h-pyrido[4,3-b]carbazoles

Modi, Sandeep P.,McComb, Todd,Zayed, Abdel-Hadi,Oglesby, R. Christopher,Archer, Sydney

, p. 5555 - 5562 (2007/10/02)

A few 6H-pyrido[4,3-b]carbazoles were prepared for cytotoxicity testing in cultures of human lung cancer cells. Methyl 6-methoxyindoleacetate 13, prepared by reduction of methyl 4-(2-nitro-5-methoxyphenyl)-3-oxobutyrate 11, was condensed with 3-acetylpyri

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