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2-Cyclohexen-1-one, 6-hydroxy-3-[(3E)-5-hydroxy-3-methyl-3-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.

80736-85-2

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80736-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80736-85-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,3 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80736-85:
(7*8)+(6*0)+(5*7)+(4*3)+(3*6)+(2*8)+(1*5)=142
142 % 10 = 2
So 80736-85-2 is a valid CAS Registry Number.

80736-85-2SDS

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-Hydroxy-3-(5-hydroxy-3-methyl-3-penten-1-inyl)-2,4,4-trimethyl-2-cyclohexen-1-on

1.2 Other means of identification

Product number -
Other names 6-Hydroxy-3-((E)-5-hydroxy-3-methyl-pent-3-en-1-ynyl)-2,4,4-trimethyl-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:80736-85-2 SDS

80736-85-2Relevant academic research and scientific papers

Technische Verfahren zur Synthese von Carotinoiden und verwandten Verbindungen aus 6-Oxo-isophoron. II. Ein neues Konzept fuer die Synthese von (3RS,3'RS)-Astaxanthin

Widmer, Erich,Zell, Reinhard,Broger, Emil Albin,Crameri, Yvo,Wagner, Hans Peter,et al.

, p. 2436 - 2446 (2007/10/02)

Starting from 6-oxo-isophorone (2) a new concept for a seven-step synthesis of (3RS,3'RS)-astaxanthin (1) has been developed.As a key feature of the new approach, the oxidation state of astaxanthin (1) is adjusted already at an early stage of the synthesis.Thus, manipulation on more complex intermediates later in the synthesis is reduced to a minimum.Acetonide 10 or dimer 13 represent the key intermediates of this concept (Scheme 2).The whole sequence has been run on a kg scale with an overall yield of 52percent (s.Scheme 5).

Process for the manufacture of cyclohexene derivatives

-

, (2008/06/13)

The compound 6-hydroxy-3-(5-hydroxy-3-methyl-1,3-pentadienyl)-2,4,4-trimethyl-2-cyclohexen-1-one useful as intermediate for producing the natural coloring agent astaxanthin as well as a method for synthesizing astaxanthin from this compound and synthesizing the compound from 2-hydroxyketo isophorone.

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