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7252-51-9

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7252-51-9 Usage

General Description

o-Nitrophenylbutylether is a chemical compound with the molecular formula C10H13NO3. It is also known as 1-(4-nitrophenoxy)butane and is a nitrophenyl ether derivative. o-Nitrophenylbutylether is commonly used in the synthesis of organic molecules and can be used as a reagent in organic chemistry reactions. It is a clear, colorless to pale yellow liquid with a slightly sweet, floral odor. o-Nitrophenylbutylether is considered to be relatively stable under normal conditions, but it is important to handle it with care and use proper safety precautions, as it can be toxic and harmful if ingested, inhaled, or absorbed through the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 7252-51-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7252-51:
(6*7)+(5*2)+(4*5)+(3*2)+(2*5)+(1*1)=89
89 % 10 = 9
So 7252-51-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO3/c1-2-3-8-14-10-7-5-4-6-9(10)11(12)13/h4-7H,2-3,8H2,1H3

7252-51-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-butoxy-2-nitrobenzene

1.2 Other means of identification

Product number -
Other names n-butyl o-nitrophenyl ether

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:7252-51-9 SDS

7252-51-9Relevant articles and documents

Boron-Promoted Ether Interchange Reaction: Synthesis of Alkyl Nitroaromatic Ethers from Methoxynitroarenes

Liu, Zhenwei,Luan, Nannan,Lu, Hongtao,Liang, Apeng,Li, Jingya,Zou, Dapeng,Wu, Yangjie,Wu, Yusheng

, p. 702 - 707 (2020/02/11)

The first protocol for boron-promoted ether interchange reaction of methoxynitroarenes was described. A series of methoxynitroarenes and alcohols, including primary, secondary, as well as tertiary alcohols were reacted smoothly in moderate to good yields under the optimized reaction conditions. This protocol constitutes an operationally simple and scalable strategy for the synthesis of alkyl nitroaromatic ethers. Moreover, the new reactivity of boron reagents was discovered.

MCM-41-immobilized 1,10-phenanthroline-copper(i) complex: A highly efficient and recyclable catalyst for the coupling of aryl iodides with aliphatic alcohols

Lin, Yang,Cai, Mingzhong,Fang, Zhiqiang,Zhao, Hong

, p. 85186 - 85193 (2016/10/12)

A heterogeneous C-O coupling reaction between aryl iodides and aliphatic alcohols was achieved in neat alcohol or toluene at 110 °C in the presence of 10 mol% of the MCM-41-immobilized 1,10-phenanthroline-copper(i) complex [MCM-41-1,10-phen-CuI] with Cs2CO3 as a base, yielding a variety of aryl alkyl ethers in good to excellent yields. The new heterogeneous copper catalyst can easily be prepared by a simple procedure from commercially available and inexpensive reagents, and recovered by filtration of the reaction solution and recycled at least 8 times without significant loss of activity.

Decarboxylative etherification of aromatic carboxylic acids

Bhadra, Sukalyan,Dzik, Wojciech I.,Goossen, Lukas J.

, p. 9938 - 9941 (2012/08/08)

Decarboxylative Chan-Evans-Lam-type couplings are presented as a new strategy for the regiospecific construction of diaryl and alkyl aryl ethers starting from easily available aromatic carboxylic acids. They allow converting various aromatic carboxylate salts into the corresponding aryl ethers by reaction with alkyl orthosilicates or aryl borates, under aerobic conditions in the presence of silver carbonate as the decarboxylation catalyst and copper acetate as the cross-coupling catalyst.

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