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(4S,5S)-(-)-5-Ethyl-2,2-dimethyl-4-(tosyloxymethyl)-1,3-dioxolan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64308-75-4

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64308-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64308-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,0 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 64308-75:
(7*6)+(6*4)+(5*3)+(4*0)+(3*8)+(2*7)+(1*5)=124
124 % 10 = 4
So 64308-75-4 is a valid CAS Registry Number.

64308-75-4Relevant academic research and scientific papers

COMPOSITION FOR ATTRACTING MALE BLUEBERRY SPANWORM MOTH

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Paragraph 0060, (2015/02/25)

A composition that includes: Z,Z-(3R,4S)-cis-3,4-epoxy-6,9-heptadecadiene; and Z,Z,Z-3,6,9-heptadecatriene, where the Z,Z-(3R,4S)-cis-3,4-epoxy-6,9-heptadecadiene and the Z,Z,Z-3,6,9-heptadecatriene are present in a ratio of between 5:1 (by mass) and about 20:1 (by mass). The composition may be for attracting a male blueberry spanworm moth. Use of a composition that includes Z,Z-(3R,4S)-cis-3,4-epoxy-6,9-heptadecadiene and Z,Z,Z-3,6,9-heptadecatriene for attracting male blueberry spanworm. A method of attracting male blueberry spanworm moths that includes placing a composition comprising Z,Z-(3R,4S)-cis-3,4-epoxy-6,9-heptadecadiene and Z,Z,Z-3,6,9-heptadecatriene suitably close to a field of having the male blueberry spanworm moths.

Formal synthesis of (+)-isolaurepinnacin

Suzuki, Toshio,Matsumura, Ryuji,Oku, Ken-ichi,Taguchi, Keiichi,Hagiwara, Hisahiro,Hoshi, Takashi,Ando, Masayoshi

, p. 65 - 67 (2007/10/03)

The stereoselective formal synthesis of (+)-isolaurepinnacin is described. The required key oxepene skeleton possessing cis-oriented alkyl substituents at the α,ω-positions was stereoselectively constructed via the cyclization of the corresponding hydroxy epoxide promoted by the (Bu3Sn)2O/Zn(OTf)2 system.

Stereoselective Acetalization of 1,1- and 1,2-Disubstituted Diols as Common Principle in the Synthesis of the Enantiomers of the Bicyclic Acetal Pheromones endo- and exo-Brevicomin and Frontalin

Wershofen, Stefan,Classen, Arnold,Scharf, Hans-Dieter

, p. 9 - 18 (2007/10/02)

The acetalization of the 1,1- and 1,2-disubstituted diols 14-19 with the keto compounds 20 and 21 has been investigated.The substitution pattern of the used diols shows great influence on the stereochemistry of the obtained dioxolanes 22-27 (mixtures of d

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