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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

-

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.

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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