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3,5,7-Octatrien-2-one, 6-methyl-8-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (3E,5Z,7E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25529-00-4

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25529-00-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25529-00-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,2 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25529-00:
(7*2)+(6*5)+(5*5)+(4*2)+(3*9)+(2*0)+(1*0)=104
104 % 10 = 4
So 25529-00-4 is a valid CAS Registry Number.

25529-00-4SDS

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-methyl-8t-(2,6,6-trimethyl-cyclohex-1-enyl)-octa-3t,5c,7-trien-2-one

1.2 Other means of identification

Product number -
Other names 3-Methyl-1t-(2.2.6-trimethyl-cyclohexen-(6)-yl)-octatrien-(1.3c.5t)-on-(7)

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:25529-00-4 SDS

25529-00-4Relevant articles and documents

β-Lactoglobulin Directed Photoisomerization of Retinal and Related Compounds

Li, Xiao-yuan,Asato, Alfred E.,Liu, R. S. H.

, p. 4841 - 4844 (1990)

The 11-cis enriched photostationary state mixture of retinal trapped in BLG, a water soluble protein, is similar to that of retinal in heptanol.The results, along with those of the lower homologs, are consistend with a model involving specific protein interaction with the cyclohexenyl portion of the substrate and remote protonation of the aldehyde carbonyl group.

A synthesis method of 9-cis Beta-carotene

-

, (2021/05/18)

The present invention relates to a method for synthesizing 9 - cis Beta-carotene (9 - cis beta-carotene) compounds having high purity and easy mass production through a chemical reaction, and a reaction for substituting 9 - cis Retinol groups of Alcohol with 9 - cis Phosphonium salt. The reaction of β - (3 - Methyl-2-butenal to Knoevenagel condensation) to synthesize All-trans Aldehyde. In step 9 - cis Retinoic Phosphonium salt) and in step), the completed All-trans Aldehyde is subjected to Wittig Olefination reaction with carbon double bonds, and 9. cis Beta-carotene obtained by the reaction of carbon double bonds.

Efficient generation of a trisporoid library by combination of synthesis and biotransformation

Schachtschabel, Doreen,Boland, Wilhelm

, p. 1366 - 1372 (2007/10/03)

(Chemical Equation Presented) Trisporic acids and their biosynthetic precursors represent a family of powerful fungal pheromones and morphogenetic factors. A highly flexible synthetic protocol is described that (i) provides rapid access to nonfunctionaliz

Syntheses of new 9- and 13-methylene isomers of retinal

Laurent,Prat,Valla,Andriamialisoa,Giraud,Labia,Potier

, p. 7221 - 7224 (2007/10/03)

Syntheses of new 9- and 13-methylene isomers of retinal via the '9-methylene-C-18 ketone' 1 or 'C-18 ketone' 2 are reported. (C) 2000 Published by Elsevier Science Ltd.

Synthesis of 9-cis-retinoic acid and C-20-[3H3C]-9-cis-retinoic acid with high specific activity

Tadikonda, Praveen K.,Lacy, James M.,Rigdon, Michael G.,Deluca, Hector F.

, p. 1 - 10 (2007/10/03)

The synthesis of 9-cis-retinoic acid starting from 2,2,6-trimethylcyclohexanone is described. The same methodology was extended for the synthesis of deuterium and tritium labeled 9-cis-retinoic acid with high specific activity (73 Ci/mmol). In this methodology, a Grignard reaction was utilized for introducing three tritium atoms simultaneously in the final synthetic steps.

Polyvinylogation Reagents: 1-Lithio-4-trimethylsiloxy-penta-1,3-diene and 1-Lithio-4-ethoxy-2-methyl-buta-1,3-diene

Duhamel, Lucette,Ancel, Jean-Erick

, p. 9237 - 9250 (2007/10/02)

Title products, lithiodienol ethers 6a and 7a, synthetic equivalents of 4-lithio pent-3-ene-2-one and 4-lithio-senecialdehyde were obtained by bromine-lithium exchange.They are choice reagents for the transformations 1 -> 2 and 1 -> 3, respectively.

Synthesis of 8-, 9-, 12-, and 13-mono-13C-retinal

Pardoen, J. A.,Mulder, P. P. J.,Berg, E. M. M. van den,Lugtenburg, J.

, p. 1431 - 1435 (2007/10/02)

The 8-, 9-, 12-, and 13-mono-13C-retinals were synthesized with >98percent chemical purity and 93percent 13C incorporation from 13C-labelled acetonitrile.Their 13C-13C and 13C-1H nmr coupling constants were determined.

A CONVENIENT ROUTE TO α,β-UNSATURATED METHYL KETONES APPLICATION TO RETINAL ANALOGUE SYNTHESIS

Croteau, Allan A.,Termini, John

, p. 2481 - 2484 (2007/10/02)

Deprotonated ketimines 1a,b add to aldehydes and ketones to provide tri- and tetra-substituted α,β-unsaturated methyl ketones 2a,b with substantial percentage of Z-geometry which are not readily accessible by other methods.

PHOTOISOMERIZATION OF THE C18 KETONE IN THE VITAMIN A SERIES. SOLVENT EFFECT ON PHOTOISOMERIZATION OF COMPOUNDS RELATED TO RETINAL

Ramamurthy, V.,Denny, M.,Liu, R. S. H.

, p. 2463 - 2466 (2007/10/02)

The directions of photoisomerization of polyenals and polyenones are believed to be controlled by the relative ordering of n,?* and ?,?* states.

4-ω-BROMOALKAPOLYENYLMETHYL KETONES-II; USE OF 5-BROMO-3-PENTEN-2-ONE ETHYLENE KETAL AS A C5-SYNTHON

Camps, J.,Font, J.,March, P. De

, p. 2493 - 2500 (2007/10/02)

The preparation of the phosphonium salt and the dimethyl-phosphonate of (E)-5-bromo-3-penten-2-one ethylene ketal, 6 and 7, is described.These C5-isoprenoid synthons were condensed with several aldehydes and ketones giving mixtures of the corresponding E

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