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(2R,3R)-threo-2-methylpentane-1,3-diol 1-benzyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78433-57-5

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78433-57-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78433-57-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,3 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78433-57:
(7*7)+(6*8)+(5*4)+(4*3)+(3*3)+(2*5)+(1*7)=155
155 % 10 = 5
So 78433-57-5 is a valid CAS Registry Number.

78433-57-5Relevant academic research and scientific papers

Versatile enantioselective synthesis of four diastereomers of serricornin, a sex pheromone of the cigarette beetle, using the SAMP/RAMP-hydrazone method

Job, Andreas,Nagelsdiek, Rene,Enders, Dieter

, p. 524 - 538 (2007/10/03)

Serricornin is a female-produced sex pheromone of the cigarette beetle (Lasioderma serricorne), which is a pest of dried foodstuffs and tobacco. We report a versatile and short synthesis of all possible 6,7-syn-isomers of serricornin, including the natura

Biosynthesis of Poriferasterol in Ochromonas malhamensis: 13C NMR Assignment of the Isopropyl Methyl Groups of 2-Methylpentan-3-ol

Colombo, Diego,Ronchetti, Fiamma,Russo, Giovanni,Toma, Lucio

, p. 962 - 964 (2007/10/02)

2-Methylpentan-3-ol stereospecifically labelled with deuterium on one of the isopropyl methyl groups has been synthesized, thus allowing the unequivocal assignmnt of their 13C NMR resonances. 13C NMR assignments for these groups proposed earlier are shown to be incorrect.Involvement in the biosynthesis of the 24β-ethylsterol poriferasterol in the crysophyte Ochromonas malhamensis is discussed.

A new synthesis of serricornin [(4s,6s,7s)-7-hydroxy-4,6-dimethyl-3-nonanone], the sex pheromone of the cigarette beetle

Mori, Kenji,Watanabe, Hidenori

, p. 3423 - 3428 (2007/10/02)

Serricornin, the sex pheromone of Lasioderma serricorne F, was synthesised in 7.6% overall yield starting from methyl (R)-3-hydroxypentanoate of microbial origin. Its (4R,6S,7S)-isomer was also synthesised.

SYNTHESIS AND ABSOLUTE STEREOCHEMISTRY OF SERRICORNIN

Mori, Kenji,Nomi, Hiroko,Chuman, Tatsuji,Kohno, Masahiro,Kato, Kunio,Noguchi, Masao

, p. 3705 - 3712 (2007/10/02)

The absolute stereochemistry of serricornin (4,6-dimethyl-7-hydroxy-3-nonanone) was established as 4S, 6S, 7S by synthesizing both (4S, 6S, 7S)-isomer and its antipode.Only the natural enantiomer was bioactive.by

DETERMINATION OF THE ABSOLUTE CONFIGURATION AT C-6 AND C-7 SERRICORNIN (4,6-DIMETHYL-7-HYDROXY-3-NONANONE), THE SEX PHEROMONE OF THE CIGARETTE BEETLE

Mori, Kenji,Nomi, Hiroko /nee Iwasawa/,Chuman, Tatsuji,Kohno, Masahiro,Kato, Kunio,Noguchi, Masao

, p. 1127 - 1130 (2007/10/02)

The absolute configuration at C-6 and C-7 of serricornin was established as (6S, 7S) by synthesizing its (6R, 7S)-erythro and (6R, 7R)-threo isomers.

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