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(S,E)-3,7,11-Trimethyl-6,10-dodecadienoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34114-96-0

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34114-96-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34114-96-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,1 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34114-96:
(7*3)+(6*4)+(5*1)+(4*1)+(3*4)+(2*9)+(1*6)=90
90 % 10 = 0
So 34114-96-0 is a valid CAS Registry Number.

34114-96-0SDS

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 (3S,6E)-3,7,11-trimethyl-dodeca-6,10-dienoic acid methyl ester

1.2 Other means of identification

Product number -
Other names (E)-(S)-3,7,11-Trimethyl-dodeca-6,10-dienoic acid methyl ester

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:34114-96-0 SDS

34114-96-0Downstream Products

34114-96-0Relevant academic research and scientific papers

Identification and Composition of Clasper Scent Gland Components of the Butterfly Heliconius erato and Its Relation to Mimicry

Darragh, Kathy,Ehlers, Stephanie,H?tling, Susan,Harig, Tim,Jiggins, Chris D.,Schulz, Stefan,Stell, Matthew,Szczerbowski, Daiane

, p. 3300 - 3313 (2021/10/12)

The butterfly Heliconius erato occurs in various mimetic morphs. The male clasper scent gland releases an anti-aphrodisiac pheromone and additionally contains a complex mixture of up to 350 components, varying between individuals. In 114 samples of five different mimicry groups and their hybrids 750 different compounds were detected by gas chromatography/mass spectrometry (GC/MS). Many unknown components occurred, which were identified using their mass spectra, gas chromatography/infrared spectroscopy (GC/IR)-analyses, derivatization, and synthesis. Key compounds proved to be various esters of 3-oxohexan-1-ol and (Z)-3-hexen-1-ol with (S)-2,3-dihydrofarnesoic acid, accompanied by a large variety of other esters with longer terpene acids, fatty acids, and various alcohols. In addition, linear terpenes with up to seven uniformly connected isoprene units occur, e. g. farnesylfarnesol. A large number of the compounds have not been reported before from nature. Discriminant analyses of principal components of the gland contents showed that the iridescent mimicry group differs strongly from the other, mostly also separated, mimicry groups. Comparison with data from other species indicated that Heliconius recruits different biosynthetic pathways in a species-specific manner for semiochemical formation.

Frogolide – An Unprecedented Sesquiterpene Macrolactone from Scent Glands of African Frogs

Menke, Markus,Melnik, Kristina,Peram, Pardha S.,Starnberger, Iris,H?dl, Walter,Vences, Miguel,Schulz, Stefan

, p. 2651 - 2656 (2018/03/29)

Some amphibians use chemical signals in addition to optical and acoustical signals to transmit information. Males of mantellid frogs from Madagascar and hyperoliid frogs from Africa emit complex, species- and sex-specific bouquets of volatiles from their femoral or gular glands. We report here on the identification, synthesis, and determination of the absolute configuration of a macrocyclic lactone occurring in several species of both families, (S)-3,7,11-dodec-6,10-dien-12-olide (S-14, frogolide). Macrolides are a preferred compound class of frog volatiles. Nevertheless, frogolide is the first macrocyclic lactone obviously derived from the terpene pathway, in contrast to known frog macrolides that are usually formed via the fatty acid biosynthetic pathway.

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