185428-55-1 Usage
Description
Tert-butyl 5-methoxy-2-nitrophenylcarbamate is a carbamate derivative featuring a tert-butyl group and a 5-methoxy-2-nitrophenyl group attached to the carbonyl carbon. It is a chemical compound primarily utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals, known for its versatility in organic synthesis to produce compounds with specific properties.
Uses
Used in Pharmaceutical Synthesis:
Tert-butyl 5-methoxy-2-nitrophenylcarbamate is used as an intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs with targeted therapeutic effects.
Used in Agrochemical Production:
tert-butyl 5-methoxy-2-nitrophenylcarbamate also serves as an intermediate in the production of agrochemicals, playing a role in the creation of substances designed to enhance crop protection and yield.
Used as a Reagent in Organic Synthesis:
Tert-butyl 5-methoxy-2-nitrophenylcarbamate is employed as a reagent in organic synthesis, where it can undergo multiple reactions to generate a range of compounds with specific applications across different industries.
It is crucial to handle tert-butyl 5-methoxy-2-nitrophenylcarbamate with care due to potential health and safety risks if mismanaged.
Check Digit Verification of cas no
The CAS Registry Mumber 185428-55-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,4,2 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 185428-55:
(8*1)+(7*8)+(6*5)+(5*4)+(4*2)+(3*8)+(2*5)+(1*5)=161
161 % 10 = 1
So 185428-55-1 is a valid CAS Registry Number.
185428-55-1Relevant articles and documents
Visible-Light-Mediated Nitration of Protected Anilines
Düsel, Simon J. S.,K?nig, Burkhard
, p. 2802 - 2807 (2018/03/09)
The photocatalytic nitration of protected anilines proceeds with riboflavin tetraacetate as an organic photoredox catalyst. Sodium nitrite serves as the NO2 source in this visible-light-driven room temperature reaction. Various nitroanilines are obtained in moderate to good yields without the addition of acid or stoichiometric oxidation agents. The catalytic cycle is closed by aerial oxygen as the terminal oxidant.
Intermediates for the synthesis of benzimidazole derivatives and a process for the preparation thereof
-
, (2008/06/13)
This invention provides a process for the preparation of a benzimidazole derivative (I) or a pharmaceutically acceptable salt thereof, 1wherein R1 is C1-C6 alkyl, C1-C6 alkoxyl, etc., R2 is C1-C6 alkyl, and R3 is hydrogen or a protecting group, which exhibits excellent hyopoglycemic action, said process comprising condensation of an amine derivative (III) with a carboxylic acid derivatives (II) to afford a compound (IV), followed by cyclization of compound (IV) in the presence of an acid.
Process for producing N-acylnitroaniline derivative
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Page 8, (2010/01/31)
A process of reacting a nitroaniline compound of formula (2); with acid anhydride or acid chloride is carried out in the presence of an alkali metal compound or an alkaline earth metal compound to produce acylnitroaniline derivative. The process further includes the step of reacting the resulting product with a compound of formula (5);R2-Y to produce an N-acylnitroaniline derivative of formula (1);
