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ethyl (2S,3S)-2-O-benzoyl-3,4-O-isopropylidene-2,3,4-trihydroxybutanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114185-08-9

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114185-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114185-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,1,8 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 114185-08:
(8*1)+(7*1)+(6*4)+(5*1)+(4*8)+(3*5)+(2*0)+(1*8)=99
99 % 10 = 9
So 114185-08-9 is a valid CAS Registry Number.

114185-08-9Relevant academic research and scientific papers

A stereocontrolled synthesis of (-)-detoxinine from L-ascorbic acid

Delle Monache, Giuliano,Misiti, Domenico,Zappia, Giovanni

, p. 2961 - 2973 (1999)

A stereoselective synthesis of (-)-detoxinine, the core unit of the detoxifying agent detoxin D1, is presented. The approach, characterized by the use of an inexpensive starting material and by the easy and stereoselective preparation of the ke

Stereoselective synthesis of the lichen metabolite, (+) montagnetol and its congeners as antimicrobial agents

Mallavadhani, Uppuluri Venkata,Boddu, Ramakrishna,Rathod, Balaji B.,Reddy Setty, Prakasam

supporting information, p. 2992 - 2999 (2018/10/15)

In view of structural diversity, (+) montagnetol, the major metabolite of the fruticose lichen, Roccella montagnei was synthesized along with three of its congeners by employing highly efficient protocols. (+) Montagnetol (2 R, 3S; 11) and (-) montagnetol (2S, 3R; 5) were synthesized in 7 and 9 steps, respectively, from L-ascorbic acid. The two new congeners 3 (2 R, 3R) and 6 (2S, 3S), which differ in configuration at C-2 and C-3 positions of the (+) montagnetol, were synthesized from (?) diethyl D-tartrate and (+) diethyl L-tartrate, respectively. The synthesized compounds were evaluated in vitro for antimicrobial activity against two Gram-positive (S. aureus and E. coli) and two Gram-negative (S. typhi and P. aeruginosa) bacteria and one fungal strain Candida albicans. Interestingly, the congener 3 showed promising anti-bacterial activity (MIC: 0.062 μg/ml) against P. aeruginosa, whereas the congener 6 displayed potent anti-fungal activity (MIC: 0.062 μg/ml) against C. Albicans.

A method of manufacturing an optical isomer [...]

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Paragraph 0043; 0044, (2017/04/11)

PROBLEM TO BE SOLVED: To asymmetrically synthesize constituent optically active substances of doranidazole and clarify pharmacological and physicochemical features of each of the optically active substances.SOLUTION: A method of producing a compound of st

A method of manufacturing an optical isomer [...]

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Paragraph 0049; 0050, (2017/05/10)

PROBLEM TO BE SOLVED: To provide a method of an asymmetric synthesis for a structural enantiomer of doranidazole, and an intermediate used for the manufacturing method.SOLUTION: There is provided a method of manufacturing 2-nitro imidazole derivative repr

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