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130694-71-2

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130694-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130694-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,9 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 130694-71:
(8*1)+(7*3)+(6*0)+(5*6)+(4*9)+(3*4)+(2*7)+(1*1)=122
122 % 10 = 2
So 130694-71-2 is a valid CAS Registry Number.

130694-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-4(Z)-(4R,5S)-4-hydroxy-4-(5-hydroxy-3-methylpent-3-en-1-ynyl)-3,3,5-trimethylcyclohexanone

1.2 Other means of identification

Product number -
Other names (4R,5S)-4-Hydroxy-4-((Z)-5-hydroxy-3-methyl-pent-3-en-1-ynyl)-3,3,5-trimethyl-cyclohexanone

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:130694-71-2 SDS

130694-71-2Downstream Products

130694-71-2Relevant articles and documents

Use of compounds to enhance synchrony of germination and emergence in plants

-

, (2008/06/13)

The present invention relates to a composition for enhancing synchrony of germination and emergence in plants and comprises an effective amount of a compound having the following general formula (I); STR1

SYNTHESIS AND BIOLOGICAL ACTIVITY OF ALLENIC ANALOGUES OF ABSCISIC ACID

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

, p. 3189 - 3195 (2007/10/02)

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.

Carotenoids and Related Compounds. Part 38. Synthesis of (3RS,3'RS)-Alloxanthin and Other Acetylenes

Davies, Anthony J.,Khare, Anakshi,Mallams, Alan K.,Massy-Westropp, Ralph A.,Moss, Gerard P.,Weedon, Basil C. L.

, p. 2147 - 2158 (2007/10/02)

The all-trans, 9-cis, and 9,9'-di-cis forms of (3RS,3'RS)-alloxanthin have been synthesized, also the 9-cis-isomer of (3RS,6'RS)-crocoxanthin.Perhydrogenation of alloxanthin gives a product with the same optical properties as perhydrozeaxanthin.These resu

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