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2-Cyclohexen-1-one, 6-(1-hydroxycyclobutyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

824975-82-8

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824975-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 824975-82-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,4,9,7 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 824975-82:
(8*8)+(7*2)+(6*4)+(5*9)+(4*7)+(3*5)+(2*8)+(1*2)=208
208 % 10 = 8
So 824975-82-8 is a valid CAS Registry Number.

824975-82-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(1-hydroxycyclobutyl)cyclohex-2-en-1-one

1.2 Other means of identification

Product number -
Other names 6-(1-hydroxycyclobutyl)cyclohex-2-enone

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:824975-82-8 SDS

824975-82-8Downstream Products

824975-82-8Relevant academic research and scientific papers

Synthesis of novel bifunctional Michael acceptors

Urbaneja, Laura Mediavilla,Krause, Norbert

, p. 4467 - 4470 (2004)

The conjugated dienones 1a, 1c-e, and 1g were synthesized by aldol reaction of cyclohex-2-enones 3 with aldehydes or ketones and subsequent elimination. Whereas the acetone adducts could be converted into the desired products 1a/g by treatment with CeCl3·7H2O/Nal, the dienones 1c-e were obtained by Appel bromination and dehydrobromination with triethylamine. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

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