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119016-09-0

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119016-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119016-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,0,1 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 119016-09:
(8*1)+(7*1)+(6*9)+(5*0)+(4*1)+(3*6)+(2*0)+(1*9)=100
100 % 10 = 0
So 119016-09-0 is a valid CAS Registry Number.

119016-09-0Relevant academic research and scientific papers

Synthesis and antimicrobial activity of novel 2-alkyl/arylcarbamato-6-(1,1-dimethylethyl)-3-cyclohexyl-3,4-dihydro-2h-1, 3,2-benzoxazaphosphorine-2-oxides

Babu, Y. Hari,Reddy, P. Vasu Govardhana,Reddy, C. Suresh,Reddy, C. Devendranath,Devi, P. Uma Maheswari

, p. 1039 - 1044 (2002)

Novel 2-alkyl/arylcarbamato-6-(1,1-dimethylethyl)-3-cyclohexyl-3,4-dihydro-2H-1, 3,2-benzoxazaphosphorine-2-oxides (IV) have been synthesized from reactions of 2-cyclohexylaminomethyl-4-t-butylphenol I [8c] with various dichlorophosphinyl carbamates (III) [8a-b] in dry toluene in the presence of triethylamine at 40-50°C. All the title compounds (IVa-j) at reflux temperature are degraded to 2-amino-6-(1,1-dimethylethyl)-3-cyclohexyl-3,4-dihydro-2H-1,3, 2-benzoxazaphosphorine-2-oxide (IVk) exclusively. The structures are determined by ir, nmr and mass spectral studies. They were screened for antifungal activity against Penicillium notatum, Aspergillus niger and Helminthosporium sps, and antibacterial activity on Escherchia coli, Staphylococcus aureus and Pseudomonas aeruginosa. A few of them possess significant activity.

Synthesis and antimicrobial activity of 2-substituted-2, 3-dihydro5-propoxy-1H-1,3,2-benzodiazaphosphole 2-oxides

Venugopal,Sankar Reddy,Devendranath Reddy,Berlin

, p. 275 - 279 (2001)

Several 2-alkylcarbamato/thiocarbamato/aryloxy/trichloromethyl-2,3-dihydro-5- propoxy-1H-1,3, 2-benzodiazaphosphole 2-oxides (4 and 6) were synthesised by reacting 4-propoxy-o-phenylenediamine (1) with various N-dichlorophosphinyl carbamates (3), aryl pho

Synthesis and Antimicrobial Activity of 8-Alkylcarbamato-16H-Dinaphtho[2,1-d:1',2'-g] 1,3,2-dioxaphosphocin 8-oxides

Babu, M. F. Stephen,Rao, L. Nagaprasada,Venugopal, M.,Raju, C. Naga,Reddy, C. Suresh

, p. 16 - 20 (2001)

A new family of phosphorus heterocycles, namely 8-alkylcarbamato-16H-dinaphto-[2,1-d:1',2'-g] 1,3,2-dioxaphosphocin 8-oxides (4a-j) has been obtained by reaction of bis(2-hydroxy-1-naphthyl)methane (3) with a series of dichlorophosphinyl carbamates (2a-j)

Synthesis, spectral, and antimicrobial activity of 6-alkylcarbamato-2,10-dichloro-12-trichloromethyl-12H-dibenzo[d,g][1, 3,2]-dioxaphosphocin 6-oxides

Kumar, K. Ananda,Kasthuraiah,Babu, M.F. Stephen,Reddy, C.Suresh

, p. 819 - 825 (2003)

6-Alkylcarbamato/alkylthiocarbamato-2,10-dichloro-12-trichloromethyl- 12H-dibenzo[d,g][1,3,2]-dioxaphosphocin 6-oxides (4a-f) have been synthesized by the condensation of 2,2-bis-(2-hydroxy-5-chlorophenyl)-1,1,1-trichloroethane (3) with dichlorophosphinyl

Synthesis, characterisation and antimicrobial activity of novel 2-alkoxycarbonylamino-1,3,2-benzodiazaphosphole 2-oxides

Reddy, P. Vasu Govardhana,Bala Krishna,Reddy, M.V. Narayana,Annar,Reddy, C. Suresh

experimental part, p. 65 - 67 (2009/10/15)

A series of some new class of 2-alkoxycarbonylamino-1,3,2- benzodiazaphosphole 2-oxides 4a-j were synthesised by reacting 3,4-diaminobenzophenone (3) with various dichlorophosphinyl carbamates (2) in drytoluene-tetrahydrofuran mixture (1:1) in the presence of triethylamine at 45-50°C. All the title compounds were evaluated for antimicrobial activity to determine their efficacy and were effective in suppressing the growth of bacteria and fungi. The chemical structures of the title products were characterised by IR, 1H, 13C and 31P NMR and mass spectral studies.

Synthesis and antimicrobial activity of 2-substituted-2,3-dihydro-1H-naphtho- [1,8-de]- 1,3,2-diazaphosphorine 2-oxides/sulfides

Venugopal,Reddy,Bavaji

, p. 822 - 827 (2007/10/03)

Several 2-alkylcarbamato/thiocarbamato/arylcarbamido/trichloromethyl/bis(2-chloro- ethyl)amino/chloroethoxy/ aryloxy-2.3-dihydro-1H-naphtho-[1,8-de]-1,3,2-diazaphosphorine 2-oxides/sulfides (4 and 6) are synthesized by reacting equimolar quantities of 1,8-diamino-naphthalene 1 with various dichlorophosphinyl carbamates/thiocarbamates/arylcarbamides 3a-1, trichloromethylphosphonic dichloride 5a, bis(2-chloroethyl)phosphoramidic dichloride 5b, O-2-chloroethyl phosphoryl chloride 5c and arylphosphorothioic dichlorides 5d-e in the presence of triethylamine at 45-65°C. Their IR, 1H, 13C, 31P NMR and mass spectral data are discussed. All these compounds are found to have significant antifungal and antibacterial activity.

Synthesis and characterization of 6-alkylcarbamato-2,10-dichloro-12H-dibenzodioxaphosphocin-6-oxides

Reddy, P. Mallikarjuna,Reddy, B. Sankara,Reddy, C. Devendranath,Berlin, K. Darrell

, p. 1085 - 1088 (2007/10/03)

Dichloroisocyanatophosphine oxide (1) on addition with alcohols/thiols give the corresponding dichlorophosphinyl carbamates/thiocarbamates (2a-j) which on condensation with 5,5'-dichloro-2,2'-dihydroxydiphenylmethane (3) afford 6-alkylcarbamato/thiocarbam

Novel Heterocycles. Synthesis of the 2,4,3-benzodiazaphosphepine Ring System

Lemke, Thomas L.,Boring, Daniel

, p. 1455 - 1456 (2007/10/02)

Novel alkyl (1,2,4,5-tetrahydro-3H-2,4,3-benzodiazaphosphepin-3-yl)carbamate-P-oxides (7) were synthesized by cyclization of the corresponding dichlorophosphinylcarbamates (5) with α,α'-diamino-o-xylene (6).A steric limitation in the synthesis of analogs

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