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1-p-Tolylpropan-1-one oxime is an organic compound with the chemical formula C10H13NO. It is a derivative of 1-p-tolylpropan-1-one, featuring an oxime functional group, which consists of a nitrogen atom double-bonded to an oxygen atom and single-bonded to a carbon atom. 1-p-tolylpropan-1-one oxime is a colorless liquid with a distinctive odor and is soluble in organic solvents. It is synthesized by reacting 1-p-tolylpropan-1-one with hydroxylamine in the presence of an acid catalyst. 1-p-Tolylpropan-1-one oxime has potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in the preparation of other organic compounds. Due to its reactivity, it should be handled with care, and appropriate safety measures should be taken during its use and storage.

54582-25-1

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54582-25-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54582-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,8 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54582-25:
(7*5)+(6*4)+(5*5)+(4*8)+(3*2)+(2*2)+(1*5)=131
131 % 10 = 1
So 54582-25-1 is a valid CAS Registry Number.

54582-25-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name p-methylpropiophenone oxime

1.2 Other means of identification

Product number -
Other names 1-p-Tolyl-propan-1-on-oxim

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:54582-25-1 SDS

54582-25-1Relevant academic research and scientific papers

Mercury-catalyzed rearrangement of ketoximes into amides and lactams in acetonitrile

Ramalingan, Chennan,Park, Yong-Tae

, p. 4536 - 4538 (2008/02/04)

(Chemical Equation Presented) An acetonitrile solution of mercury(II) chloride has been found to catalyze efficiently the conversion of a diverse range of ketoximes into their corresponding amides/lactams.

Aluminium chloride promoted carbohydroximoylation reaction of aromatic compounds with primary nitroalkanes

Kim,Song,Ryu

, p. 1711 - 1715 (2007/10/02)

The reaction of primary nitroalkanes with aromatic compounds in the presence of aluminium chloride afforded the corresponding carbohydroximoylated aromatic compounds.

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