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(+)-<2R,6S,S(R)>-6-(tert-Butyldimethylsilyloxy)-1-(p-tolylsulfinyl)-heptan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

158930-52-0

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158930-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 158930-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,9,3 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 158930-52:
(8*1)+(7*5)+(6*8)+(5*9)+(4*3)+(3*0)+(2*5)+(1*2)=160
160 % 10 = 0
So 158930-52-0 is a valid CAS Registry Number.

158930-52-0Downstream Products

158930-52-0Relevant academic research and scientific papers

Compound and application of compound in preparation of orseolia oryzae sex attractant

-

, (2016/12/22)

The invention discloses a compound and an application of the compound in preparation of an orseolia oryzae sex attractant. The compound is (6S)-6-acetoxyl-2-heptanone, and a structural formula of the compound is represented as a formula I. The compound can cooperate with (6S)-6-acetoxyl-2-heptanone to be taken as the orseolia oryzae sex attractant or can be independently taken as the orseolia oryzae sex attractant, and the compound can be used for performing population monitoring and comprehensive control of orseolia oryzae. The orseolia oryzae sex attractant prepared from the compound and a lure of the orseolia oryzae sex attractant can be applied to: (1) orseolia oryzae population monitoring and prediction; (2), mass trapping; (3), mating disruption. The sex attractant prepared from the sex pheromone (namely, the compound) and the lure of the sex attractant can be used for performing population monitoring and comprehensive control on the orseolia oryzae, and the sex attractant has the advantages of low cost and high efficiency and is suitable for predicting the occurrence rule of pests hiding in insect galls.

Compound and application thereof to preparation of orseolia oryzae wood-mason sex attractant

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, (2017/04/03)

The invention discloses a compound and application thereof to preparation of orseolia oryzae wood-mason sex attractant. The compound is (2S, 6S)-2, 6-2 acetoxyl group heptanes, and the structural formula of the compound is as shown in the formula I. The compound can be matched with (6S)-6-acetoxyl group-2-heptanone or used independently to serve as the orseolia oryzae wood-mason sex attractant and can be used for conducting population monitoring and comprehensive prevention and control over orseolia oryzae wood-mason. The orseolia oryzae wood-mason sex attractant prepared from the compound and a lure of the sex attractant can be used for population monitoring and predication of orseolia oryzae wood-mason, mass trapping and interference with mating. The sex attractant prepared from sex pheromone (compound) and the lure of the sex attractant can be used for population monitoring and comprehensive prevention and control over orseolia oryzae wood-mason, and the sex attractant is low in cost, high in efficiency and suitable for predicating occurrence regularity of pests hiding in insect galls.

Rice gall midge sex attractant and application thereof

-

Paragraph 0048-0049, (2017/04/03)

The invention discloses rice gall midge sex attractant and application thereof.The rice gall midge sex attractant is prepared from two rice gall midge sex pheromone effective components, namely, (2S,6S)-2,6-Diacetoxyheptane and (6S)-6-acetoxyl group-2-hep

Asymmetric synthesis of solenopsins A, B and C

Solladie, Guy,Huser, Nathalie

, p. 153 - 156 (2007/10/02)

Solenopsins A, B and C have been synthesized in enantiomerically pure forms from the corresponding anti-1,5-diols which have been obtained from glutaric anhydride by an asymmetric synthesis induced by chiral sulfoxides.

Asymmetric synthesis of both enantiomers of 2.5-hexane diol and 2.6-heptane diol induced by chiral sulfoxides

Solladie, Guy,Huser, Nathalie,Garcia-Ruano, Jose Luis,Adrio, Javier,Carmen Carreno,Tito, Amelia

, p. 5297 - 5300 (2007/10/02)

both enantiomers of 2,5-hexane diol and 2,6-heptane diol have been prepared respectively by stereoselective reduction of optically active diketodisulfoxides and ketosulfoxides.

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