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p-nitrobenzyl 2-<2-oxo-3α-bromo-4-(benzothiazol-2-yldithio)azetidin-1-yl>-2-isopropenylacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95122-89-7

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95122-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95122-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,1,2 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 95122-89:
(7*9)+(6*5)+(5*1)+(4*2)+(3*2)+(2*8)+(1*9)=137
137 % 10 = 7
So 95122-89-7 is a valid CAS Registry Number.

95122-89-7Relevant academic research and scientific papers

Process for preparation of penam derivatives

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Page/Page column 4; sheet 1, (2008/06/13)

The invention relates to novel processes for preparing penam derivatives, such as Tazobactam and derivatives thereof. The processes according to the invention encompass procedures for the protection and deprotection of the carboxylic group as well as for the oxidation of the sulfur moiety of penam derivatives. Additionally, the present invention relates to new intermediates for the production of penam derivatives, allowing the desired penam-derivatives to be formulated with high purity and in good yields.

Process for preparation of penam derivatives

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Page/Page column 7-8, (2008/06/13)

The invention relates to novel processes for preparing penam derivatives, such as Tazobactam and derivatives thereof. The processes according to the invention encompass procedures for the protection and deprotection of the carboxylic group as well as for the oxidation of the sulphur moiety of penam derivatives. Additionally, the present invention relates to new intermediates for the production of penam derivatives, allowing the desired penam-derivatives to be formulated with high purity and in good yields.

A novel, mild, and facile method to prepare 6-methylidene pe nem derivatives

Abe, Takao,Sato, Chisato,Ushirogochi, Hideki,Sato, Koichi,Takasaki, Tsuyoshi,Isoda, Takeshi,Mihira, Ado,Yamamura, Itsuki,Hayashi, Kazuhiko,Kumagai, Toshio,Tamai, Satoshi,Shiro, Motoo,Venkatesan, Aranapakam M.,Mansour, Tarek S.

, p. 5850 - 5860 (2007/10/03)

A novel and mild method was established to synthesize 6-methylidene penem compounds. This method entails a MgBr2/Et3N-promoted aldol-type condensation on 6-bromopenem 12 with an appropriately substituted aldehyde to yield the interme

Process for preparing 6-alkylidene penem derivatives

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, (2008/06/13)

The present invention provides a process of making compounds of formula I, which are useful for the treatment of bacterial infection or disease.

PROCESS FOR PREPARING 6-ALKYLIDENE PENEM DERIVATIVES

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Page/Page column 46, (2010/02/07)

The present invention provides a process of making compounds of Formula (I), which are useful for the treatment of bacterial infection or disease.

Synthesis and β-lactamase inhibitory properties of 2β-[(acyloxy)methyl]-2-methylpenam-3α-carboxylic acid 1,1-dioxides

Gottstein,Haynes,McGregor

, p. 518 - 522 (2007/10/02)

p-Nitrobenzyl 2β-[(benzoyloxy)methyl]-2α-methylpenam-3α-carboxylate was prepared by reaction of p-nitrobenzyl 2-[2-oxo-3α-bromo-4-(benzothiazol-2-yldithio)acetidin-1-yl]-2-isopropenyl acetate with silver benzoate in the presence of iodine. The resulting d

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