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50352-33-5

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50352-33-5 Usage

General Description

2-(Benzyloxy)-4-nitrophenol is a chemical compound with the molecular formula C13H10N2O5. It is a yellow crystalline solid with a molecular weight of 266.23 g/mol. 2-(Benzyloxy)-4-nitrophenol is used in various chemical reactions and processes as an intermediate or starting material. It is also used in the synthesis of other organic compounds and pharmaceuticals. It is important to handle 2-(Benzyloxy)-4-nitrophenol with care, as it is potentially hazardous and should be used in a well-ventilated area with appropriate protective equipment.

Check Digit Verification of cas no

The CAS Registry Mumber 50352-33-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,3,5 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 50352-33:
(7*5)+(6*0)+(5*3)+(4*5)+(3*2)+(2*3)+(1*3)=85
85 % 10 = 5
So 50352-33-5 is a valid CAS Registry Number.

50352-33-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitro-2-phenylmethoxyphenol

1.2 Other means of identification

Product number -
Other names (5-Nitro-2-hydroxy-phenyl)-benzyl-aether

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:50352-33-5 SDS

50352-33-5Relevant articles and documents

Preparation and unequivocal identification of the regioisomers of nitrocatechol monobenzyl ether

Bolchi, Cristiano,Bavo, Francesco,Pallavicini, Marco

supporting information, p. 1507 - 1513 (2017/08/16)

The four positional isomers of nitrocatechol monobenzyl ether were prepared as intermediates to nitrobenzodioxanes directly from 2-benzyloxyphenol or, through two-four steps, from catechol. These preparations addressed the issue of the certain identificat

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