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2-Cyclohexen-1-one, 6-hydroxy-3-(3-hydroxy-3-methyl-4-penten-1-ynyl)-2,4,4-trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83020-62-6

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83020-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83020-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,2 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83020-62:
(7*8)+(6*3)+(5*0)+(4*2)+(3*0)+(2*6)+(1*2)=96
96 % 10 = 6
So 83020-62-6 is a valid CAS Registry Number.

83020-62-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Hydroxy-3-(3'-hydroxy-3'-methyl-4'-penten-1'-inyl)-2,4,4-trimethyl-2-cyclohexen-1-on

1.2 Other means of identification

Product number -
Other names 6-hydroxy-3-(3-hydroxy-3-methyl-pent-4-en-1-ynyl)-2,4,4-trimethyl-2-cyclohexen-1-one

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:83020-62-6 SDS

83020-62-6Relevant academic research and scientific papers

METHOD FOR PRODUCING ASTAXANTHIN AND CANTHAXANTHIN INTERMEDIATE PRODUCTS

-

Page/Page column 12, (2008/06/13)

The invention relates to a method for producing cyclohexenone derivatives of general formula (I), wherein R1 represents hydrogen or OH; R2 represents (Ia), comprising the following steps: (a) hydrolyzing a cyclohexenol compound of fo

Technische Verfahren zur Synthese von Carotinoiden und verwandten Verbindungen aus 6-Oxo-isophoron. V. Synthese von Astacin

Widmer, Erich,Lukac, Teodor,Bernhard, Kurt,Zell, Reinhard

, p. 671 - 683 (2007/10/02)

Starting from optically inactive astaxanthin intermediates, the highly oxygenated carotenoid astacene was synthesized in seven steps (55percent overall yield from 6-oxo-isophorone).Key features of the new approach are base- and acid-catalyzed rearrangements of acetylenic intermediates such as those described in Schemes 2, 7 and 8.

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