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56968-86-6

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56968-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56968-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,6 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56968-86:
(7*5)+(6*6)+(5*9)+(4*6)+(3*8)+(2*8)+(1*6)=186
186 % 10 = 6
So 56968-86-6 is a valid CAS Registry Number.

56968-86-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-5-oxocyclohepta-1,3,6-triene-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-hydroxy-5-oxo-cyclohepta-1,3,6-trienecarboxylic acid

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:56968-86-6 SDS

56968-86-6Relevant articles and documents

Synthesis of α-Tropolones through Autoxidation of Dioxole-Fused Cycloheptatrienes

Berkowitz, Alex J.,Murelli, Ryan P.

, (2022/02/07)

Herein, we describe the formation of tropolones through the autoxidation of Büchner reaction-derived cycloheptatrienes. The reaction is exceptionally simple procedurally, as it involves blowing a stream of compressed air over the cycloheptatriene, and the products can be obtained without any need for chromatography. The chemistry works specifically on dioxolane-fused systems or close variants, and substitution patterns are also important. A radical-based mechanistic hypothesis is put forward to explain these results. Finally, we demonstrate the utility of the overall process in the synthesis of amide-appended tropolones and an isomer of stipitatic acid.

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