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3,5-Di-tert-butyl-4-hydroxybenzaldehyde oxime is an organic compound with the chemical formula C14H23NO2. It is a derivative of 4-hydroxybenzaldehyde, featuring two tert-butyl groups at the 3rd and 5th positions, and an oxime functional group. 3,5-Di-tert-butyl-4-hydroxybenzaldehyde oxime is known for its antioxidant properties and is commonly used as a stabilizing agent in polymers, plastics, and rubber to prevent degradation caused by heat, light, and oxygen exposure. It is also used in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical structure. The compound is characterized by its pale yellow color and a melting point of around 180-190°C. Its chemical stability and reactivity make it a valuable intermediate in the chemical industry.

787-13-3

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787-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 787-13-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 787-13:
(5*7)+(4*8)+(3*7)+(2*1)+(1*3)=93
93 % 10 = 3
So 787-13-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H23NO2/c1-14(2,3)11-7-10(9-16-18)8-12(13(11)17)15(4,5)6/h7-9,16,18H,1-6H3

787-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-ditert-butyl-4-[(hydroxyamino)methylidene]cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 4-hydroxy-3,5-di-tert-butylbenzaldehyde 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:787-13-3 SDS

787-13-3Relevant articles and documents

Derivatives of 2-(iminomethyl)amino-phenyl, their preparation, their use as medicaments and the pharmaceutical compositions containing them

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Page column 108, (2008/06/13)

A compound selected from the group consisting of a compound of the formula wherein A is selected from the group consisting of and the other substituents are defined in the specification having an inhibitory activity of NO-synthase enzymes producing nitrogen mono-oxide and/or an activity which traps the reactive oxygen species.

Hydroxy- or methoxy-substituted benzaldoximes and benzaldehyde-O-alkyloximes as tyrosinase inhibitors

Ley, Jakob P,Bertram, Heinz-Jürgen

, p. 1879 - 1885 (2007/10/03)

Several benzaldoximes, benzaldehyde-O-ethyloximes, and acetophenone-oximes were synthesized and evaluated as tyrosinase inhibitors by an assay based on tyrosinase catalyzed L-DOPA oxidation. Whereas benzaldoxime itself is only a weak inhibitor, its deriva

Some heterocyclic derivatives of sterically hindered phenols

Bannikov,Ershov,Nikiforov

, p. 410 - 413 (2007/10/03)

Five- and six-membered heterocyclic compounds containing sterically hindered phenols as structural fragments were obtained by dipolar 1,3-cycloaddition of substituted nitrile oxides to olefins, azomethines, and acetylenes.

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