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N-[1,2-bis(4-methoxyphenyl)ethylidene]hydroxylamine is a complex organic compound with the chemical formula C17H18N2O3. It is characterized by a hydroxylamine group (NHOH) attached to a central ethylidene (CH2) unit, which is flanked by two 4-methoxyphenyl rings. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates due to its unique structure and reactivity. The presence of the methoxy groups on the phenyl rings can influence the compound's solubility and electronic properties, making it a versatile building block in organic chemistry.

5471-45-4

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5471-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5471-45-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,7 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5471-45:
(6*5)+(5*4)+(4*7)+(3*1)+(2*4)+(1*5)=94
94 % 10 = 4
So 5471-45-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H17NO3/c1-19-14-7-3-12(4-8-14)11-16(17-18)13-5-9-15(20-2)10-6-13/h3-10,18H,11H2,1-2H3

5471-45-4SDS

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 N-[1,2-bis(4-methoxyphenyl)ethylidene]hydroxylamine

1.2 Other means of identification

Product number -
Other names Deoxyanisoin oxime

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:5471-45-4 SDS

5471-45-4Relevant academic research and scientific papers

Catalyst free synthesis of mono- and disubstituted pyrimidines from O-acyl oximes

Upare, Atul,Sathyanarayana, Pochampalli,Kore, Ranjith,Sharma, Komal,Bathula, Surendar Reddy

supporting information, p. 2430 - 2433 (2018/05/23)

Transition-metal or iodine catalyzed transformations of O-acyl oximes to various N-heterocycles are well established. Herein, we report a catalyst free, oxime carboxylate based, three-component condensation method to access mono- and disubstituted pyrimidines. A broad range of substituted pyrimidines were prepared in moderate to excellent yields. Control experiments reveal that in situ generated formamidine is the key intermediate.

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