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99530-30-0

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99530-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99530-30-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,5,3 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 99530-30:
(7*9)+(6*9)+(5*5)+(4*3)+(3*0)+(2*3)+(1*0)=160
160 % 10 = 0
So 99530-30-0 is a valid CAS Registry Number.

99530-30-0Relevant academic research and scientific papers

Preparation of the enantiomers of hydroxy-C18 fatty acids and their anti-rice blast fungus activities

Kato, Tadahiro,Nakai, Toshio,Ishikawa, Rumiko,Karasawa, Aya,Namai, Tsuneo

, p. 2695 - 2701 (2007/10/03)

In order to examine the correlation between the anti-rice blast fungus activity and the chirality of allylic alcohols 1-3, which were characterized from the infected rice plants as an enantiomeric mixture with 10% e.e., a procedure for the chemical prepa

Production of hydroxy unsaturated fatty acids using crude lipoxygenase obtained from infected rice plants

Kato, Tadahiro,Watanabe, Tsutomu,Hirukawa, Toshifumi,Tomita, Norihiro,Namai, Tsuneo

, p. 1663 - 1666 (2007/10/03)

In order to explore the oxidation mode of lipoxygenase (LOX) obtained from infected rice plants, typical unsaturated fatty acids (3-8) were treated with LOX and oxygen. It was observed that ω-10 and ω-6 positions of unsaturated fatty acids were oxidized predominantly in the cases of exotic ω-6 (4 and 5) and ω-3 (7 and 8) series, respectively. In the case of endogenous fatty acids (3 and 6), oxidation at ω-6 position predominated. All the allylic alcohols obtained by reduction of the oxidation products with NaBH4 possess S-configuration.

Stereospecific Total Synthesis of Dimorphecolic Acid, 5(S)-HETE, and 12(S)-Hete

Shimazaki, Toshiyuki,Kobayashi, Yuichi,Sato, Fumie

, p. 1785 - 1788 (2007/10/02)

First enantiospecific synthesis of dimorphecolic acid is accomplished via an efficient and stereocontrolled route.The convenient synthesis of 5(S)-HETE and 12(S)-HETE is also described.

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