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2,4,6,8-Nonatetraenal, 3-(1,1-dimethylethyl)-7-methyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (E,E,Z,E)is a complex polyunsaturated aldehyde with a unique structure and functional groups. It contains four double bonds, a t-Bu group, a methyl group, and a cyclohexenyl group. The (E,E,Z,E) notation represents the configuration of the double bonds in the molecule. Due to its reactivity and potential toxicity, caution should be exercised when handling and using this chemical.

113775-89-6

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113775-89-6 Usage

Uses

Used in Organic Synthesis:
2,4,6,8-Nonatetraenal, 3-(1,1-dimethylethyl)-7-methyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (E,E,Z,E)is used as a key intermediate in the synthesis of various organic compounds. Its unique structure and functional groups make it a valuable building block for the development of new molecules with potential applications in various fields.
Used in Biochemistry:
In biochemistry, 2,4,6,8-Nonatetraenal, 3-(1,1-dimethylethyl)-7-methyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (E,E,Z,E)can be used as a probe to study the interactions of biomolecules with aldehydes. Its reactivity and functional groups allow it to form covalent bonds with proteins, nucleic acids, and other biomolecules, providing insights into the molecular mechanisms of various biological processes.
Used in Material Science:
2,4,6,8-Nonatetraenal, 3-(1,1-dimethylethyl)-7-methyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (E,E,Z,E)can be utilized in the development of advanced materials with unique properties. Its polyunsaturated structure and functional groups can be incorporated into polymers, coatings, and other materials to enhance their performance, such as improving their thermal stability, mechanical properties, or chemical resistance.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,4,6,8-Nonatetraenal, 3-(1,1-dimethylethyl)-7-methyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (E,E,Z,E)can be employed as a starting material for the synthesis of bioactive compounds with potential therapeutic applications. Its unique structure and functional groups can be exploited to design and develop new drugs with improved efficacy and selectivity.
Used in Flavor and Fragrance Industry:
2,4,6,8-Nonatetraenal, 3-(1,1-dimethylethyl)-7-methyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (E,E,Z,E)can be used as a building block for the creation of novel fragrances and flavors. Its complex structure and functional groups can contribute to the development of unique and appealing scents and tastes, enhancing the sensory experience of various consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 113775-89-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,7 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 113775-89:
(8*1)+(7*1)+(6*3)+(5*7)+(4*7)+(3*5)+(2*8)+(1*9)=136
136 % 10 = 6
So 113775-89-6 is a valid CAS Registry Number.

113775-89-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E,4Z,6E,8E)-3-tert-Butyl-7-methyl-9-(2,6,6-trimethyl-cyclohex-1-enyl)-nona-2,4,6,8-tetraenal

1.2 Other means of identification

Product number -
Other names -

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:113775-89-6 SDS

113775-89-6Relevant academic research and scientific papers

Retinoids. 6. Preparation of alkyl- and trimethylsilyl-substituted retinoids via conjugate addition of cuprates to acetylenic esters

Ernst, Ludger,Hopf, Henning,Krause, Norbert

, p. 398 - 405 (2007/10/02)

Five retinoids bearing the ethyl, tert-butyl, and trimethylsilyl groups in the 9-position of retinal and the ethyl and tert-butyl groups in the 13-position have been synthesized. The key step of the syntheses involves the conjugate addition of lithium die

19,19,19- AND 20,20,20-TRIMETHYLRETINAL: SIDE CHAIN TERT-BUTYL SUBSTITUTED RETINALS

Lera, Angel R. de,Okamura, William H.

, p. 2921 - 2924 (2007/10/02)

The 11-cis, 13-cis, 11,13-dicis, and 9,11,13-tricis isomers of 19,19,19-trimethylretinal (1) and the 13-cis and 11,13-dicis isomers of 20,20,20-trimethylretinal (2) were synthesized and characterized.The Dess-Martin reagents is an effective oxidant for the retinol to retinal conversion.

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