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benzyl methylphosphonochloridate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122086-11-7

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122086-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122086-11-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,0,8 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 122086-11:
(8*1)+(7*2)+(6*2)+(5*0)+(4*8)+(3*6)+(2*1)+(1*1)=87
87 % 10 = 7
So 122086-11-7 is a valid CAS Registry Number.

122086-11-7Relevant academic research and scientific papers

Evaluation of phosphorus-containing inhibitors of γ-glutamyl hydrolase

Rodriguez, Chester E.,Holmes, H. Michael,Mlodnosky, Karyn L.,Lam, Vinh Q.,Berkman, Clifford E.

, p. 1521 - 1524 (1998)

Several putative, phosphorus-containing inhibitors of γ-glutamyl hydrolase were synthesized and evaluated for inhibitory activity. The phosphonamidoic acids were shown to be weak competitive inhibitors while both a phosphoramidate diester and a phosphonamidate ester were shown to be potent time-dependent inactivators, presumably through irreversible phosphorylation of an active site nucleophile.

PHOSPHONATES SYNTHONS FOR THE SYNTHESIS OF PHOSPHONATES DERIVATIVES SHOWING BETTER BIOAVAILABILITY

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Page/Page column 13; 16-17, (2010/12/31)

Synthons for the synthesis of phosphonates prodrugs POM and POC, especially for direct Cross Metathesis.

α-haloenamines as reagents for the conversion of phosphorus oxyacids to their halogenated analogues

Norlin, Rikard,Juhlin, Lars,Lind, Per,Trogen, Lars

, p. 1765 - 1770 (2007/10/03)

Phosphorus oxyacids are converted to their halogenated analogues under mild conditions. α-Haloenamines are shown to be effective halogen transfer reagents affording good to high yields of the desired products at reaction times, in some cases, less than one minute. Georg Thieme Verlag Stuttgart.

A convenient two-step one-pot synthesis of phosphonamidates

Mlodnosky, Karyn L.,Holmes, H. Michael,Lam, Vinh Q.,Berkman, Clifford E.

, p. 8803 - 8806 (2007/10/03)

Phosphonamidates are formed in high yield from a one-pot sequential reaction of a phosphonyl dichloride with an alcohol and then an amine in the presence of catalytic 1H-tetrazole. Undesired disubstitution of the phoshphonyl dichloride by the alcohol or the amine is minimal due to the presence of tetrazole.

Synthesis and evaluation of a polyamine phosphinate and phosphonamidate as transition-state analogue inhibitors of spermidine/spermine-N1-acetyltransferase

Wu, Ronghui,Saab, Nada H.,Huang, Huatao,Wiest, Laurie,Pegg, Anthony E.,Casero Jr., Robert A.,Woster, Patrick M.

, p. 825 - 836 (2007/10/03)

Polyamine analogues such as bis(ethyl)norspermine and N1-ethyl-N11-[(cyclopropyl)methyl]-4,8-diazaundecane (CPENSpm) act as inhibitors of the enzyme spermidine/spermine-N1-acetyltransferase (SSAT) in vitro and possess impr

Convenient "one-pot" synthesis of chlorophosphonates, chlorophosphates and chlorophosphoramides from the corresponding benzyl esters

Saady, Mourad

, p. 4785 - 4786 (2007/10/02)

Selective monodeprotection of alkyl phosphonate, phosphate and phosphoramide benzyl esters using quinuclidine and chlorination of the subsequent salts allows preparation of various alkyl phosphonochloridates, monochlorophosphates and monochlorophosphoramides in a convenient "one-pot" procedure.

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