Abstract: A multifunctional spool tool having a body with winding edges for winding a utility cord thereabout, and one or more of: a lighter clip and lighter, a cutting blade, a notch for fusing the utility cord, or a supplemental component such as a flashlight, compass, knife, fire starter, magnifying glass, screwdriver, measuring device, pen, storage device, magnesium striker, can opener, safety belt knife, skinning knife, tweezers, toothpick, or a signal mirror.

Abstract: A multifunctional spool tool having a body with winding edges for winding a utility cord thereabout, and one or more of: a lighter clip and lighter, a cutting blade, a notch for fusing the utility cord, or a supplemental component such as a flashlight, compass, knife, fire starter, magnifying glass, screwdriver, measuring device, pen, storage device, magnesium striker, can opener, safety belt knife, skinning knife, tweezers, toothpick, or a signal mirror.

Abstract: A multifunctional spool tool having a body with winding edges for winding a utility cord thereabout, and one or more of: a lighter clip and lighter, a cutting blade, a notch for fusing the utility cord, or a supplemental component such as a flashlight, compass, knife, fire starter, magnifying glass, screwdriver, measuring device, pen, storage device, magnesium striker, can opener, safety belt knife, skinning knife, tweezers, toothpick, or a signal mirror.

Abstract: There are described intermediates for the preparation of known pyrazoloazole photographic magenta dye forming couplers and processes for making and using these intermediates. The intermediates are low molecular weight compounds represented by the structure: ##STR1## wherein: R, X, R.sup.1 and Y are defined herein. The process for making these intermediates involves diazotizing a 5-amino-1H-pyrazole to produce a 5-diazo-1H-pyrazole, then condensing the diazotized product with an active methine or methylene compound having a pKa of 14 or less to produce a substituted hydrazone and then subjecting the hydrazone to cyclization and reduction, in either order.

Abstract: A process for making a compound of formula III ##STR1## wherein R.sub.6 is a group bonded to the rest of the molecule by a carbon atom;R.sub.3 is a group containing a carbon atom and bonded to the rest of the molecule by a carbon atom or by a heteroatom; andX is hydrogen or a substituent, comprising:reacting with hydrazine a compound of formula II ##STR2## or a dehydrated analog of formula II, wherein R.sub.3, R.sub.6, and X have the same meaning as for formula III, and Y is a nucleofugal leaving group.

Abstract: Novel pyrazolotriazole dye-forming couplers contain an aliphatic or aromatic aryl ballast group and having one carboxy or sulfonic group on the ballast group enabling the pyrazolotriazole to have increased activity and having an ether (--O--) group or group A bonded directly to a carbon atom or arylene group that is bonded directly to the pyrazolotriazole nucleus and wherein the pyrazolotriazole is capable of forming an immobile dye in a gelatino silver halide emulsion and is free of coupling-off groups that reduce silver. When the ballast group is bonded to the pyrazoloazole nucleus by means of an aromatic group, the aromatic group is ortho substituted. Group A is ##STR1## --S--, --SO--, --SO.sub.3 --, or --OSO.sub.2 --. The ether group or group A enables the dye formed to have desired hue. These couplers are useful in photographic silver halide materials and processes.