Abstract: The present invention relates to a high-concentration starch adhesive prepared by treating a starch slurry at a temperature of 100.degree. C. or above to form a gelatinized solution and suspending an ungelatinized starch in the gelatinized solution. According to the present invention, the viscosity of the starch adhesive can be kept stable over a long period of time; the problems such as warp due to the expansion and contraction, by the absorption of water, of the material to be adhered, can be solved; and the quantity of heat necessitated in the adhesion step can be much reduced.

Abstract: The present invention relates to a high concentration aqueous starch slurry adhesive comprising 20 to 60% of starch and the following components in the specified amount based on the weight of starch:(1) 0.01 to 1.0% of rhamsan gum or xanthan gum,(2) 1.0 to 3.0% of sodium hydroxide, and(3) if necessary, up to 3% of sodium tetraborate.According to the present invention, a high concentration aqueous starch slurry adhesive can be easily obtained at a single step by merely dispersing starch into cold water while stirring.

Abstract: 4-Anilinoquinazoline derivatives of formula (I): ##STR1## (in which: R.sup.1 represents a hydrogen atom, a halogen atom, a trifluoromethyl group or a nitro group;R.sup.2 represents a hydrogen atom, a C.sub.1 -C.sub.4 alkyl group, an alkoxy group or a halogen atom; andR.sup.3 represents a hydrogen atom cr a C.sub.1 -C.sub.4 alkyl group)and pharmaceutically acceptable salts thereof are, except where R.sup.1 represents a hydrogen atom or a chlorine atom in the 6- position when R.sup.2 and R.sup.3 both represent hydrogen atoms, new compounds and have been found to possess valuable analgesic and anti-inflammatory activities. These compounds can be prepared by heating the appropriate 4-haloquinazoline with an appropriate aniline or aniline derivative.

Abstract: Thiophene derivatives of the formula ##STR1## wherein X, Y and Z are as herein defined, said compounds being useful as fungicides, are described.

Abstract: Agricultural fungicidal compositions containing as an active ingredient one or more 4-aminoquinazoline derivatives. The amino group is substituted, e.g., with a phenoxyalkylene, and the quinazoline nucleus may be substituted at 2- and or 6-positions.

Abstract: A method of using 4-anilinoquinazoline derivatives of formula (I): ##STR1## (in which: R.sup.1 represents a hydrogen atom, a halogen, atom, a trifluoromethyl group or a nitro group;R.sup.2 represents a hydrogen atom, a C.sub.1 -C.sub.4 alkyl group, an alkoxy group or a halogen atom; andR.sup.3 represents a hydrogen atom or a C.sub.1 -C.sub.4 alkyl group)and pharmaceutically acceptable salts thereof are, provided that R.sup.1 does not represents a hydrogen atom or a chlorine atom in the 6- position when R.sup.2 and R.sup.3 both represent hydrogen atoms, as an analgesic and anti-inflammatory in the treatment of mammals. These compounds can be prepared by heating the appropriate 4-haloquinazoline with an appropriate aniline or aniline derivative.

Abstract: 4-Aminoquinazoline derivatives of formula (I): ##STR1## (wherein: R.sup.1 represents an alkyl group, a cycloalkyl group, an alkenyl group or a benzyl group;R.sup.2 and R.sup.3 are the same or different and each represents a hydrogen atom, an alkyl group, an alkoxy group or a halogen atom;X represents a straight or branched chain alkylene group; andn is 0 or 1)and salts and hydrates thereof are valuable fungicidal, anti-insect (insect-repellent and insecticidal) and acaricidal compounds and thus can be used to treat or prevent many diseases affecting agricultural and horticultural plants, while, at the same time, having a much lower toxicity to fish than is exhibited by other known compounds.

Abstract: New diphenyl ether derivatives having one to three substituents selected from a halogen atom and a trifluoromethyl group at any optional one to three positions of the 2'-, 3'-, 4'-, 5'- and 6'-positions in one phenyl moiety and nitro group at the 4-position and unsubstituted or substituted aminosulfonyl group at the 3-position in another phenyl moiety. They have a superior herbicidal effect and can be prepared starting from a known 3-benzylmercapto compound through three steps.

Abstract: Agricultural fungicidal compositions containing as an active ingredient one or more 4-aminoquinazoline derivatives. The amino group is substituted, e.g., with a phenoxyalkylene, and the quinazoline nucleus may be substituted at 2- and or 6-positions.

Abstract: In a process for preparing an o-alkoxy-p-allylphenol comprising reaction of an o-alkoxyphenol with an allyl halide in the presence of an aqueous solution of an alkali metal hydroxide or alkaline earth metal hydroxide, the improvement which comprises employing a copper-containing compound such as a water-soluble copper salt, an ammine copper complex salt etc., as the catalyst. The process for preparing an o-alkoxy-p-allylphenol which comprises reaction of an o-alkoxyphenol with an allyl halide in an aqueous ammonia is also disclosed.

Abstract: Process for preparing monoalkyl ethers of dihydric phenols using a catalyst comprising Al, B and P.