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27241-90-3

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27241-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27241-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,2,4 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27241-90:
(7*2)+(6*7)+(5*2)+(4*4)+(3*1)+(2*9)+(1*0)=103
103 % 10 = 3
So 27241-90-3 is a valid CAS Registry Number.

27241-90-3SDS

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 4-bromo-N-[(E)-(4-methoxyphenyl)methylideneamino]aniline

1.2 Other means of identification

Product number -
Other names Anisal-4-brom-phenylhydrazin

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:27241-90-3 SDS

27241-90-3Downstream Products

27241-90-3Relevant articles and documents

N-Aminations of Benzylamines and Alicyclic Amines with Nitrosoarenes to Hydrazones and Hydrazides

Jana, Chandan K.,Purkait, Anisha

, p. 2687 - 2696 (2019/06/19)

Unlike other alkylamines, benzylamines upon reaction with a nitrosoarene undergo oxidation to the corresponding imines. A direct amination of benzylamines, which was difficult to achieve due to its facile oxidation, to the corresponding hydrazones is reported. A wide variety of benzylamines and N-heterocycles were reacted with nitrosoarenes to provide structurally diverse hydrazones and hydrazides, respectively. Moreover, the direct N-amination reaction was applied to the one-pot synthesis of triazoles.

Synthesis, crystal structure, optical and electrochemical properties of novel diphenylether-based formazan derivatives

Turkoglu, Gulsen,Berber, Halil,Kani, Ibrahim

supporting information, p. 2728 - 2740 (2015/04/14)

In this study, formazans 5a-5h were synthesized by coupling the reactions of substituted phenylhydrazone compounds 3a-3h with diazonium salt of 4-chloro-2-phenoxybenzenamine (4). The substituted phenylhydrazones 3a-3h were obtained from the condensation o

A new route to substituted pyrimido[5,4-e]-l,2,4-triazine-5,7(1H,6H)-diones and facile extension to 5,7(6H,8H) isomers

Turbiak, Anjanette J.,Showalter, H. D. Hollis

experimental part, p. 4022 - 4026 (2010/03/30)

A new route to substituted pyrimido[5,4-e]-l,2,4-triazine-5,7(lH,6H)-diones is outlined. The synthesis proceeds via preformed hydrazone intermediates, which are then condensed with an activated chlorouracil to build up the entire molecular framework, foll

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