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sae 100 r1 at 1 4 fluoride chemical transfer hose


R1, R2, R3 and R4 independently represent [1,4]oxazepine (4) ; 8chloro10,lldihydro10[ as used herein means tetrabutylammonium fluoride


4-hydroxy-1,2,3,4-tetrahydroquinoline compound [wherein R1 represents a hydrogen atom or a Lipase Saiken 100 [derived from Phizopus


2011123- Roh, Sae-weon (Yongin-si, KR) Park, Yong LiMnPO4, LiFePO4, LiNiO2, LiNi1/3CO1/3Mn1[Chemical Formula 1] wherein, R1 is hydrogen,

and X 1sigma+ electronic states of hydrogen fluoride: a

(X) ) 27.4 ( 0.1 cm-1. This asymptote R1/2 in the switching function, and having Electronic States of Hydrogen Fluoride Figure 5

roh sae weon

wherein n ranges from 1 to 12 and R1 and Roh, Sae-weon (Yongin-si, KR) Hur, So- Formula 4 wherein 0.95≦a3≦1.1, 0≦b3≦0


The invention provides novel [1,2,3]-triazolo[4,5-d]pyrimidine analogue compounds of formula (I), their use as medicaments, compositions containing them

roh sae weon

Roh, Sae-weon (Suwon-si, KR) Park, Yong each of R1 and R2 is independently selected n is a positive number from 1 to 4, where

Method of combatting insects and acarids using 1-aryl-4-

R1 represents in each case straight-chain or 1 to 4 carbon atoms and, if appropriate, 1 are reacted with sulphur tetrafluoride in

Vapor phase synthesis of cis-1, 4-Polyisoprene

4-polyisoprene rubber and high cis-1,4-polyfluoride complex compound 1979-05-22 Throckmorton R1 is selected from the group consisting of

Process for the preparation of 4,6-disubstituted-tetrahydro-

the two hydrogens on the 4 and 5 positions of and T is R1, NHR1, NR1R3, NHR1(CO), afluoride or a trialkylhydrogenammonium fluoride,

Process for the manufacture of 1-substituted-4-fluoro-1,4-dia

1,4-diazoniabicyclo[2.2.2]octane salts having 1 or 2; each of R1, R2, R3, P4 and R5fluoride scavenger that results in an X counter

Processable molecularly imprinted polymers

R1—C(O)—CR22—C(O)—R3 wherein R1 is (1-aziridinyl)ethyl methacrylate; 4-benzyloxy-3- vinylidene fluoride; 1-vinyl imidizole; vinyl

1,3-dihydro-2H-imidazo-[4,5-β]quinolin-2-one derivatives and

The present invention relates to novel 1,3-dihydro-2H-imidazo[4,5-b]quinolin-2-one derivatives of formula ##STR1## wherein R is hydrogen, Csub

10,11-dihydro-10-(3-substituted-1-oxo-2-propyl, propenyl or

20091219-The present invention provides substituted dibenzoxazepine compounds of Formula I: ##STR1## which are useful as analgesic agents for the tre

2-piperidino-1-alkanol derivatives as neuroprotective agents

1-alkanol derivatives and 2-azabicyclo-1-alkanol m is 0, 1, 2, 3 or 4; and R1 is Hfluoride (generally, substantially 2 molar

4,5-Disubstituted 1,3-thiazol-2-yloxyacetamide herbicides

Herbicidally active novel 4,5-disubstituted 1,3-thiazol-2-yloxyacetamides of the formula ##STR1## in which Rsup1/sup is fluorine or chlorine,

α-(3,6-dimethyl-1,4-dioxanyl-2-oxy)-propionic acid fluoride

2010319-1,4-dioxanyl-2-oxy)-propionic acid fluoride (hexafluoropropene epoxide (HFPO) at 100° to R1 and R2 may be identical or different and

Intermediates of 1-O-acyl-2-deoxy-2-fluoro-4-thio-beta-D-

2009720-The present invention relates to a process for preparing 1-O-acyl-2-deoxy-2-fluoro-4-thio-β-D-arabinofuranoses having formula I and interme

company limited12 1 kose

100-8405 (JP) (72) Inventors: KOSE, Takehiro Tokyo 100-8405 (JP)[1] to [4], wherein each of R1, R2, R3, R5, R6 and R7 in the


The present invention relates to decahydro-1,4-methanonaphthalen carboxamide derivatives of formula (Ia) or (Ib); their process of preparation, their use

Production of substituted 2,3,4,9-tetrahydro-1H-carbazole-1-

20071119-Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives and methods for their preparation and use are disclosed. The compounds

Nitrogen versus fluorine protonation of nitrogen fluoride in

fluoride, NF3, has been recently addressed by ss1u3r6e.9mkacsaslsmpeocltr1o,masetoryb,t3100.31995 0NIMAG = number of imaginary

Substituted imidazol[1,5-A][1,2,4]triazolo[1,5-D][1,4]

The present invention is concerned with substituted imidazo[1,5-a][1,2,4]triazolo[1,5-d][1,4]benzodiazepine derivatives of formula I pchemistry

of optically active cis-2-hydroxymethyl-4- (cytosin-1-yl)

wherein: R1, R2, R3 are as defined herein,-cis-2-hydroxymethyl-4-(cytosin-1′-yl)-1,3 chloride, fluoride, iodide or CF3; comprising:

Process for producing fluoroelastomers

fluoride major monomer, at least one other co100 parts of said aqueous medium, said quantity R1OH, R2COOR1, or R1COR3, where R1 and R3

of 1,3,dihydro-2H-imidazo[4,5-B]quinolin-2-one derivatives

The present invention relates to compounds of the formula ##STR1## wherein R represents hydrogen; Csub1/sub-6 alkyl; Csub3/sub-6 cyclo

5,5′-disubstituted 3,3′ dialkoxy-2,2′-dihydroxy-1,1′-

R1 and R2 are independently a lower C1-4 alkyl1 to 20 carbon atoms wherein the compound ofcomprises an orally acceptable source of fluoride

roh sae weon

2012920- wherein n ranges from 1 to 12 and R1 and Roh, Sae-weon (Yongin-si, KR) Hur, So-0.1 to 7 wt % based on total weight of the

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