Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Silane, Dichloro-

Silane Dichloro-ethyl-trifluoro-methyl- ElOb, 435 (Br - Si) c3hsf... [Pg.591]

Silane (Dichloro-fluoro-niethyl)-trimethyl- ElOb,. 407/413 (Educt)... [Pg.606]

Silane, chlorodimethyloctyl-. See Octyidimethylchlorosilane Silane, chlorodimethylvinyl- Silane, chloroethenyidimethyl-. See Vinyidimethylchlorosilane Silane, chloromethylphenyl-. See Phenylmethylchlorosilane Silane, (3-cyanopropyl) trichloro-. See 3-Cyanopropyltrichlorosilane Silane, decyltrichloro-. See n-Decyltrichlorosilane Silane, dichloro-. See Dichlorosilane Silane, dichlorodiethyl-. See Diethyidichlorosilane... [Pg.3908]

Methyl vinyl dichlorosilane (dichloro methyl vinyl silane) [124-70-9] M 141.1, b 43-45.5 /ll-11.5mm, 91 /742mm, 92.5 /743.2mm, 92.5-93 /atm, d 1.0917, n 1.444. Likely impurities are dichloromethylsilane, butadienyl-dichloromethylsilane. Fractionate through a column packed... [Pg.442]

Diethylcadmium (in finely-divided state) Iron disulphide Dichloro(methyl)silane... [Pg.189]

Alkylation Conditions of Bf nzene Derivatives (R-Ph) wmi (DICHLOROAL.KYL)SILANES (ChX Si(CH2) CX-Cl2) AND PRODUCT YIELDS... [Pg.171]

A regio- and stereospecific INOC reaction of unsymmetrical silaketals 114, synthesized in one pot from unsaturated alcohols, nitro ethanol, and dichloro-silanes, via the nitrile oxide 115 to isoxazolines 116 has been described (Scheme 14) [37a]. The intermolecular version of the cycloaddition, under similar conditions, proceeds with poor regio and stereoselectivity. [Pg.16]

There are reactive softeners, some of which are N-methylol derivatives of long-chain fatty amides (10.241) while others are triazinyl compounds (10.242). The N-methylol compounds require baking with a latent acid catalyst to effect reaction, whereas dichloro-triazines require mildly alkaline fixation conditions. The N-methylol compounds are sometimes useful for combination with crease-resist, durable-press, soil-release and water-repellent finishes. In this context, the feasibility of using silane monomers such as methyltri-ethoxysilane (10.243), vinyltriethoxysilane (10.244), vinyl triace tylsilane (10.245) and epoxypropyltrimethoxysilane (10.246) in crosslinking reactions to give crease-resist properties and softness simultaneously has been investigated [492]. [Pg.264]

We found that dichloro diorgano silanes are suitable reagents for the synthesis of diorgano bis(0-alkyl)phosphonates. A different reactivity of both chlorine atoms of the silanes is observed in the dealkylation reaction of dialkylphosphonates in contrast to Me3SiBr [2]. [Pg.75]

The enhanced reactivity of the chlorine atom in the dichloro diorgano silanes can also be observed in Me2(MeO)SiCl 4 or Me(EtO)2SiCl 5. In both cases the O-alkyl O-silylphosphonates (6, 7) are formed in high yields after reaction of 4 or 5 with dialkyl phosphonates. [Pg.76]

The successful trapping of di-E-butylsilylene from a dichloro-silane suggested the possibility of a general reaction mechanism. [Pg.220]

See other pages where Silane, Dichloro- is mentioned: [Pg.578]    [Pg.1047]    [Pg.104]    [Pg.205]    [Pg.306]    [Pg.407]    [Pg.551]    [Pg.647]    [Pg.660]    [Pg.671]    [Pg.685]    [Pg.788]    [Pg.133]    [Pg.198]    [Pg.199]    [Pg.200]    [Pg.1276]    [Pg.89]    [Pg.135]    [Pg.578]    [Pg.1047]    [Pg.104]    [Pg.205]    [Pg.306]    [Pg.407]    [Pg.551]    [Pg.647]    [Pg.660]    [Pg.671]    [Pg.685]    [Pg.788]    [Pg.133]    [Pg.198]    [Pg.199]    [Pg.200]    [Pg.1276]    [Pg.89]    [Pg.135]    [Pg.76]    [Pg.441]    [Pg.365]    [Pg.543]    [Pg.145]    [Pg.152]    [Pg.215]    [Pg.362]    [Pg.427]    [Pg.429]    [Pg.175]    [Pg.175]    [Pg.175]    [Pg.257]    [Pg.617]    [Pg.56]    [Pg.174]   
See also in sourсe #XX -- [ Pg.6 , Pg.39 ]



SEARCH



© 2024 chempedia.info