1sn r1at en 853 1 sn hose for phosphoric acid

Process for the manufacture of mixed phosphoric acid ester

Mixed phosphoric acid ester compositions containing by weight less than 4% of a triaryl phosphate; from about 30% to about 35% of an aryl dialkoxy

Certain phosphoric acid ester derivatives of 1,3-dioxy propane

Certain phosphoric acid ester derivatives of 1,3- ##STR1## wherein R1 is tridecyl or of 1,2-isopropylidene-3-tetradecyl-sn-glycerol

Use of 1,3,4-oxa- or thiadiazol-2-yl-(thio)phosphoric acid

Use of 1,3,4-oxa- or thiadiazol-2-yl-(thio)phosphoric acid triamide X, Y = O or S; R1, R2 = H; or 1-8C alkyl/heteroalkyl, 2-8C

ammonium salt phosphoric acid ester as conditioner for hair

Use of long carbon chain quaternary ammonium salt phosphoric acid ester of formula (I) as conditioner for hair. pchemistry id=CHEM-US-00001 num

Phosphoric compound, method for preparing the same, and flame

an integer of 1 to 3, wherein R1 is phenyl.at a temperature of about 120 to about 160° (D1) an aromatic phosphoric acid ester compound,

(R1R2R3)–N+/H3PO4 composite membrane for phosphoric acid

A poly(R sub1/sub R sub2/sub R sub3/sub )–N sup+/sup /H sub3/sub PO sub4/sub composite membrane has

Oximinophosphoric acid derivatives, and their use for

Oximinophosphoric acid derivatives of the formula ##STR1## where Rsup1/sup is a straight-chain or branched alkyl of not more than 4 carbon

Asymmetric O,S-dialkyl dithiophosphoric acid esters of 1,2,3-

Benztriazinonylmethyl-organophosphoric esters of the formula ##EQU1## wherein Rsub1/sub represents ethyl, propyl, isopropyl, n-butyl, i-butyl or

Phosphoric acid monoester salts, process for their

R1 is a straight or branched chained alkyl having 1 to 13 carbon atoms, More particularly, the new phosphoric acid monoester salts of the present

2,2-Dichlorocyclopropyl-methyl-phosphoric acid derivatives

2,2-Dichlorocyclopropylmethyl-phosphoric acid derivatives of the formula I ##STR1## where Rsup1/sup, Rsup2/sup and Rsup3/sup are

1--D-5-(HsDXR1)

phosphoric acid catalyst Renier Schwarzera, Elizabeth du Toita and Willie that both the equilibrium reactions – r1 and r3 – are slightly exothermic

AZETIDINONE DERIVATIVES AS BETA-LACTAMASE INHIBITORS

Abstract not available for EP1012139brAbstract of corresponding document: strongUS5994340/strongbrNew 2-oxo-1-azetidine sulfonic acid derivatives

Phosphoric acid group-containing non-aqueous dispersion and a

This invention relates to a phosphoric acid group-containing non-aqueous dispersion wherein polymer particles are dispersed in a solution of a macromolecular

Phosphoric acid esters, process for their preparation and use

Phosphoric acid esters and their salts corresponding(-O-) and at least one carboxylic acid ester in which R1 is an alkyl group with 1 to 4

-3-,,,1--3-,,,

20081119-O,O-Dialkyl-O-(1-phenyl-2-carbalkoxyvinyl)-thionophosphoric acid esters of the formula ##STR1## in which R, Rsub3/sub and Rsub4/

5-Chloro-1,2,4-triazolyl phosphoric acid derivs. - used as

5-Chloro-1,2,4-triazolyl phosphoric acid derivs. - used as pesticides, In (I), R1 is 1-6C alkyl; R2 is 1-6C alkyl, 1-6C alkoxy, 1-6C

Molecular probes and modulators for PI-PLC and PI 3-kinase

(d) R1=RC(═O) or R, R2=R′C(═O) orat least one additional hydroxyl group derivatized phosphoric acid (15) and 1-O-hexanoyl-2-O-(

of cyclic imides in the presence of polyphosphoric acid

(C═O)—R1, alkyl is unbranched or branched alkyl having 1-6 C atomspolyphosphoric acid to give the corresponding N-(nitroaryl)cycloimide

peptides and proteins by reacting with a phosphoric acid

A peptide or protein is modified by reacting a phosphoric acid ester (I) with a peptide or protein: ##STR1## wherein R1 means a linear

alkylthiocarbonyl and aminocarbonyl)-2-phosphorus acid ester

Phosphoric acid esters of the formula ##STR1## wherein X is CH or N, p Ar is optionally substituted phenyl, diphenyl or naphthyl, /pp

Cyclopropylmethylphosphoric acid derivatives

New phosphoric acid derivatives, a process for their manufacture by reaction of cyclopropylmethyl halides with salts of phosphoric acid derivatives, and

pyridinyloxy)ethoxy]-2-pyrazinylpiperazine L-malate for

acid and R1-R4 are each independently selected (2R)-methyl-1-{3-[2-(3-pyridinyloxy)ethoxy formula HA in step (iii) is phosphoric acid

Process for the preparation of phosphoric acid derivatives

R1 and R2 comprising alkyl with 1 to 4 carbon in the presence of an inorganic base at a pyrimidinylphosphoric acid derivatives, intermediate

Amidino-phosphoric acid thiol esters for combating pests

Amidino-phosphoric acid thiol esters hereinafter defined in formula I are useful as active ingredients in pesticidal compositions containing them. They are