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Biphenyls diamino

Hetero-substituted 4,7-diarj lbenzofuroxans (Section V,C) are known. The only representative 5-arylbenzofuroxan in Table I is 5,5 -bisbenzofuroxanyl (23), prepared from 4,4 -diamino-3,3 -dinitro-biphenyl by oxidation with hypochlorite. [Pg.15]

Dimethylamino-methyl)-2-hydroxymethyl-aus 2 -Carboxy-2-(dimethylaminocarbonyl)-biphenyl und Lithiumalanat 165 2,2 -Dinitro- 474, 476, 695 6,6 -Dinitro-2,2 -bis-[chlorcarbonyl]- 188 2,2 -Dinitro-4,4 -bis-[diathylamino]- 695 4,4 -Dinitro-2,2 -bis-rhydroxymethyl]- 213 6,6 -Dinitro-2,2 -bis-[hydroxymethyl]- 188 2,2 -Dinitro-4,4 -diamino- 695 6,6 -Dinitro-2,2 -diformyl- 694 4,4 -Dinitro-2,2 -dimethoxycarbonyl- 213 2,2 -Dinitro-4,4 -dimethyl- 695 6,6 -Dinitro-2 -formyl-2-carboxy- 694 2,2 -Dinitroso- 476 -4-hydroxamsaure-chlorid 537 4-(a-Hydroxy-benzyl)- 542 Methoxy- 678 2-Methyl- 556 Nitro- 672, 678 4-Nitro- 687... [Pg.976]

Scott et al. [45] prepared diimine derivatives of 2,2 -diamino-6,6 -dimethyl-biphenyl (as structure 37 in Scheme 19) as copper chelates for the catalyzed cyclopropanation reaction. All catalysts were active in this reaction but enan-tioselectivities varied importantly according to the substitution pattern of the imine aryl group only ortho-substituted ligands (by chloride or methyl groups) led to products with measurable enantioselectivity for the model test reaction (up to 57% ee with 37). [Pg.108]

Reported structures for homobifunctional aryl azides include a biphenyl derivative and a naphthalene derivative (Mikkelsen and Wallach, 1976), a biphenyl derivative containing a central, cleavable disulfide group (Guire, 1976), and a compound containing a central l,3-diamino-2-propanol bridge between phenyl azide rings that are nitrated (Guire, 1976). The only commercially available homobifunctional photoreactive crosslinker is BASED. [Pg.262]

Principally, one commercially available sulfonated diamine (4,4 -diamino-2,2 -biphenyl disulfonic acid) has been used to synthesize sulfonated polyimides. In addition to the commercially available diamine, several novel sulfonated diamines incorporating flexible or kinked structures have been prepared in Okamoto s lab. " The chemical structures and names of all five diamines are shown in Figure 23. [Pg.360]

Synonyms AI3-00140 Azoic diazo component 112 Benzidine base p-Benzidine Benzioine 4,4 -Bianiline p,//-Bianiline (l,l -Biphenyl)-4,4 -diamine 4,4 -Biphenyldiamine p,//-Biphenyl-diamine 4,4 -Biphenylenediamine p,//-Biphenylenediamine BRN 0742770 CCRIS 71 C.I. 37225 C.I. azoic diazo component 112 4-Diaminodiphenyl jo-Diaminodiphenyl 4,4 -Diamino-biphenyl p,//-Diaminobiphenyl 4,4 -Diamino-l,l -biphenyl 4,4 -Diaminodiphenyl p.p -Di-aminodiphenyl 4,4 -Dianiline p,/y-Dianiline 4,4 -Diphenylenediamine p,//-Diphenylenedi-amine EINECS 202-199-1 Fast corinth base B NCI-C03361 NSC 146476 RCRA waste number U021 UN 1885. [Pg.129]

Synonyms BRN 2108022 CCRIS 220 C.I. 23060 Curithane C126 DCB 4,4 -Diamino-3,3 -di-chlorobiphenyl 4,4 -Diamino-3,3 -dichlorodiphenyl Dichlorobenzidine Dichlorobenzidine base m m -Dichlorobenzidine 3,3 -Dichloro-l,r-(biphenyl)-4,4 -diamine 3,3 -Dichlorobiphenyl-4,4 -diamine 3,3 -Dichloro-4,4 -biphenyldiamine 3,3 -Dichloro-4,4 -diaminobiphenyl 3,3 -Di-chloro-4,4 -diamino(l,1-biphenyl) EINECS 202-109-0 NSC 154073 RCRA waste number U073. [Pg.403]

Developer 13, see p-Phenylenediamine Developer P, see 4-Nitroaniline Developer PF, see p-Phenylenediamine Devicarb, see Carbaryl Devikol, see Dichlorvos Devol orange B, see 2-Nitroaniline Devol orange R, see 3-Nitroaniline Devol orange salt B, see 2-Nitroaniline Devol red GG, see 4-Nitroaniline Devoran, see Lindane Devoton, see Methyl acetate Diacetone, see Diacetone alcohol Diacetonyl alcohol, see Diacetone alcohol Diakon, see Methyl methacrylate Dialene 6, see 1-Hexene 1,4-Diaminobenzene, see p-Phenylenediamine p-Diaminobenzene, see p-Phenylenediamine 4-Diaminodiphenyl, see Benzidine p-Diaminodiphenyl, see Benzidine 4,4 Diaminobiphenyl, see Benzidine p,p -Diaminobiphenyl, see Benzidine 4,4 -Diamino-l,l -biphenyl, see Benzidine 4,4 -Diamino-3,3 -dichlorobiphenyl, see 3,3 -Dichloro-benzidine... [Pg.1475]

Dichloro-2-chloroethylene, see Trichloroethylene 3,3 -Dichloro-4,4 -diamino-(l,1-biphenyl), see 3,3 -Di-... [Pg.1475]

Allerdings ist die Reaktion auch bei anderen Anilinen erfolgreich. So erhalt man z. B. aus 4,4 -Diamino-3,3, 5,5 -tctrachlor-biphenyl mit Chromsaureanhydrid in 70" heiBer Es-sigsaure 4,4 -Bis- 4 -amino-2,3, 5, 6-tetrachlor-4-hiphenylylazo -3,3, 5,5 -tetrachlor-biphe-nyl ... [Pg.71]

Biological significance can sometimes arise in rather unexpected ways the thermal properties of chelate polymers of 2,6-diaminopimelic acid (dap 12) and 4,4 -diamino-3,3 -dicarboxybiphenyl (bbdc 13) with Zn11 have been compared241 with those of non-polymeric divalent metal chelates with amino acids. This confirms the expected enhancement of thermal stability when coordination polymerization occurs, these results possibly being relevant to the thermal stability of certain bacterial spores which contain dap. Zn11 complexes of dap are more thermally stable than those of bbdc, possibly because the latter chelate cannot pack as well, due to the intermolecular repulsions of the biphenyl groups. [Pg.939]

Exercise 23-36 Treatment of a mixture of 2,2 dimethylhydrazobenzene and hydrazo-benzene with acid gives only 4,4 -diaminobiphenyl and 4,4 -diamino-2,2 -dimethyl-biphenyl. What does this tell you about the mechanism of this type of rearrangement Write a mechanism for the rearrangement of hydrazobenzene that is in accord with the acid catalysis (the rate depends on the square of the H concentration) and the lack of mixing of groups as described above. [Pg.1141]

Synonyms 4,4 -biphcnyldiaminc 4,4 -diamino-l, 1 -biphenyl, p,//-dianiline Formula C12H12N2 MW 184.26 Structure ... [Pg.287]

Common Name 3,3 -Dichlorobenzidine Synonym 3,3 -dichloro-4,4 -diamino(l,l -biphenyl), DCB Chemical Name 3,3 -dichlorobenzidine CAS Registry No 91-94-1... [Pg.98]

Starting materials and solvents were purchased from Aldrich Chemical Co. acetonitrile (ACN), N,N-dimethylformamide (DMF), and N-methyl-2-pyrrolidone (NMP) were obtained anhydrous in Sure/Seal bottles and used as received. The polyamic acid of PMDA-ODA (2545 Pyralin) was supplied by DuPont. The soluble polyimide XU-218, derived from 3,3, 4,4 -benzophenone tetracarboxylic dianhydride (BTDA) and diamino-1,1,3-trimethyl-3-phenylindan isomers (DAPI) was purchased from Ciba-Geigy Corp. The acetylene terminated imide oligomer powder (Thermid MC-600) derived from BTDA, aminophenylacetylene, and 1,3-bis (2-aminophenoxy) benzene (APB) was obtained from National Starch and Chemical Company. Kapton Type II (PMDA-ODA) films were obtained from DuPont Co., Apical polyimide films were obtained from Allied Corp., and Upilex Type-S and Type-R polyimide films derived from 3,3, 4,4 -biphenyl tetracarboxylic dianhydride (BPDA) plus p-phenylenediamine (PDA) and ODA, respectively were obtained from ICI Americas Inc. [Pg.395]

BENZYDYNA (POLISH) p,p-BIANILINE 4,4 -BIANILINE (l,T-BIPHENYL)-4,4 -DIAMINE (9CI) 4,4 -BIPHENYLDIAMINE 4,4 -BIPHENYLENEDIAMINE C.I. 37225 C.I. AZOIC DIAZO COMPONENT 112 p,p -DIAMINOBIPHENYL 4,4 -DIAMINOBIPHENYL 4,4 -DIAMINO-l,T-BIPHENYL p-DIAMINODIPHENWL 4,4 -DIAMINODIPHENYL p,p -DIANILINE 4,4 -DIPHENYLENEDIAMINE FAST CORINTH BASE B NCI-C03361 RCRA WASTE NUMBER U021... [Pg.140]

SYNS C.I. 23060 CURITHANE C126 DCB 4,4 -DIA DNO-3,3 -DICHLOROBIPHENYL 4,4 -DIAMINO-3,3 -DICHLORODIPHENYL 3,3 -DICHLORBENZIDIN (CZECH) 3,3 -DICHLOROBENZIDINA (SPANISH) DICHLOROBENZIDINE o,o -DICHLOROBENZIDINE 3,3 -DICHLOROBENZIDINE DICHLOROBENZIDINE BASE 3,3 -DICHLOROBIPHENYL-4,4 -DIAMINE 3,3 -DICHLORO-4,4 -BIPHENYLDIAMINE 3,3 -DICHLORO-4,4 -DIAMINOBIPHENYL 3,3 -DICHLORO-4,4 -DIAMINO(l,l-BIPHENYL) RCRA WASTE NUMBER U073... [Pg.455]

SYNS BIANISIDINE 4,4 -BI-o-TOLUIDINE C.I. 37230 C,I. AZOIC DIAZO COMPONENT 113 (4,4 -DI-AMINE)-3,3 -DIMETHYL(l,l -BIPHENYL) 4,4 -DIAM-INO-3,3 -DIMETHYLBIPHENYL 4,4 -DIAMINO-3,3 -DI-METHYLDIPHENYL DIAMINODITOLYL 3,3 -DI-METHYLBENZIDIN 3,3 -DIMETHYI.BENZIDINE 3,3 -DLMETHYL-4,4 -BIPHENYLDIAMINE 3,3 -DI-xMETHYLBIPHENYL-4,4 -DIAMINE 3,3 -DIMETHYL-(l,l -BIPHENYL)-4,4 -DIAMINE 3,3 -DIMETHYL-4,4 -DI-PHENYLDIAMINE 3,3 -DIMETHYLDIPHENYL-4,4 -DI-AMINE 4,4 -DI-o-TOLUIDINE FAST DARK BLUE BASE R RCRA WASTE NUMBER U095 o-TOLIDIN 2-TOLIDIN (GERMAN) 2-TOLIDINA (ITALIAN) TOLIDINE o,o -TOLIDINE 2-TOLIDINE 3,3 -TOLIDINE... [Pg.1350]

DIAMINOBENZIDENE see BGK500 3,3 -DIAMINOBENZIDINE TETRAHYDROCHLORIDE see BGK750 6,6 -DIANnNO-m,m -BIPHENOL see DMI400 4,4 -DIAMINOBIPHENYL see BBXOOO p,p -DIAMINOBIPHENYL see BBXOOO 4,4 -DIAMINO-l,l -BIPHENYL see BBXOOO 4,4 -DIAMINOBIPHENYL-3,3 -DICARBOXYLIC ACID see BFX250... [Pg.1611]


See other pages where Biphenyls diamino is mentioned: [Pg.215]    [Pg.215]    [Pg.91]    [Pg.282]    [Pg.51]    [Pg.210]    [Pg.359]    [Pg.359]    [Pg.360]    [Pg.223]    [Pg.547]    [Pg.71]    [Pg.72]    [Pg.90]    [Pg.741]    [Pg.742]    [Pg.24]    [Pg.44]    [Pg.292]    [Pg.1138]    [Pg.579]    [Pg.309]    [Pg.242]    [Pg.38]    [Pg.5277]    [Pg.981]    [Pg.995]    [Pg.997]   
See also in sourсe #XX -- [ Pg.1455 ]




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Biphenyl 4,4 -diamino

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