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Acetic acid (E)-3-methyl-5-(2,6,6-trimethyl-4-oxo-cyclohex-1-enyl)-pent-2-en-4-ynyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137349-53-2

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137349-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137349-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,3,4 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 137349-53:
(8*1)+(7*3)+(6*7)+(5*3)+(4*4)+(3*9)+(2*5)+(1*3)=142
142 % 10 = 2
So 137349-53-2 is a valid CAS Registry Number.

137349-53-2Downstream Products

137349-53-2Relevant academic research and scientific papers

SYNTHESIS AND BIOLOGICAL ACTIVITY OF ALLENIC ANALOGUES OF ABSCISIC ACID

Abrams, Suzanne R.,Milborrow, B. V.

, p. 3189 - 3195 (1991)

Key Word Index - Lemma gibba; Lemnaceae; abscisic acid; ABA; ABA analogue; allene; turion; growth inhibition.Abstract - Novel allenic analogues of abscisic acid (ABA) were synthesized and tested for ABA activity.The allene functional group was introduced by one of two methods: base catalysed isomerization of an enyne to an enallene conjugated to a ketone, or reduction of a 2-butyn-1,4-diol to an allenic alcohol.A 3:1 mixture of (E)- and (Z)-3-methyl-5-(4',4'-ethylenedioxy-2',6',6'-trimethylcyclohex-2'-en-1'-ylidene)-2,4,5-pentatrienoic acids strongly inhibited growth of axenic duckweed (Lemna gibba) causing a 50percent reduction in frond number at 60 μgl-1 over 7 days in continuous light.Racemic ABA caused the same inhibition at 130 μgl-1.The mixture caused the production of turion-like structures, an effect known hitherto to be induced only by short photoperiods or by certain concentrations of ABA.

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