21440-96-0

Usage

InChI:InChI=1/C10H11NO2/c1-10(2)7-5-3-4-6-8(7)11-9(12)13-10/h3-6H,1-2H3,(H,11,12)

Upstream product

• 1009367-84-3 4-iodomethyl-4-methyl-1,4-dihydro-2H-3,1-benzoxazin-2-one 
• 490035-94-4 tert-butyl N-[2-(1-methylethenyl)phenyl]carbamate 
• 75-44-5 phosgene 
• 15833-00-8 o-aminophenyldimethylcarbinol 
• 551-93-9 2-aminoacetophenone 
• 530-62-1 1,1'-carbonyldiimidazole 
• 201230-82-2 carbon monoxide 
• 100476-16-2 2-(2-Nitrophenyl)-2-propanol 

Downstream Products

• 21440-97-1 brofoxine 
• 328955-86-8 6-Amino-1,4-dihydro-4,4-dimethyl-1,3-benzo[d]oxazin-2-one 

Relevant academic research and scientific papers

Donor-Acceptor Materials Exhibiting Thermally Activated Delayed Fluorescence Using a Planarized N-Phenylbenzimidazole Acceptor

An N-phenylbenzimidazole constrained in a coplanar fashion with a methylene tether (IMAC) was designed and used to prepare a series of emitters exhibiting thermally activated delayed fluorescence (TADF). Four novel TADF emitters using 9,9-dimethylacridine

HIGH STRESS RESISTANT PLANT GROWTH REGULATOR AND PREPARATION METHOD AND USE THEREOF

Disclosed are a high stress resistant plant growth regulator and a preparation and use thereof. In particular, the compound provided by the present invention is an ABA substitute for significantly improving the stress resistance of plants, and therefore has a very wide application prospect.

CARBAMATE QUINABACTIN

The present invention relates to novel sulfonamide derivatives, to processes and intermediates for preparing them, to plant growth regulator compositions comprising them and to methods of using them for controlling the growth of plants, improving plant tolerance to abiotic stress (including environmental and chemical stresses), inhibiting seed germination and/or safening a plant against phytotoxic effects of chemicals.

Intramolecular conversion of N,N-bis(2-picolyl)ureas to cyclic carbamates

Herein, we present a new methodology for preparing 6-membered ring carbamates from a CuI-promoted cyclization of N,N-bis(2-picolyl)amine substituted ureas. The reactions work best in the presence of up to five-fold excess of CuCl at room temper

Synthesis of 1,4-dihydro-2H-3,1-benzoxazin-2-ones by hydriodic acid mediated cyclization of t-butyl 2-vinylphenylcarbamates

A two-step facile synthesis of 4,4-disubstituted 1,4-dihydro-2H-3,1- benzoxazin-2-ones starting from α-substituted 2-aminostyrenes is described. The method involves the hydriodic acid mediated cyclization of t-butyl 2-vinylphenylcarbamate derivatives, whi

Convenient synthesis of 1,4-dihydro-2H-3,1-benzoxazin-2-ones by iodocyclization of t-butyl 2-vinylphenylcarbamates

It has been found that t-butyl 2-vinylphenylcarbamate derivatives underwent iodocyclization on treatment with iodine in the presence of sodium hydrogencarbonate to afford 4-iodomethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one derivatives in generally good yields. The reduction of these 4-iodomethyl derivatives with tributyltin hydride gave the corresponding 4-methyl derivatives in good yields.

Novel combinations of medicaments for the treatment of respiratory diseases containing long-acting beta-agonists and at least one additional active ingredient

Disclosed are medicament combinations which contain in addition to one or more, preferably one, compound of general formula 1 wherein the groups X, Ra, Rb, R1, R1′, R2, R2′, R2″,

SAR studies of 6-(arylamino)-4,4-disubstituted-1-methyl-1,4-dihydro-benzo[d][1,3]oxazin-2-ones as progesterone receptor antagonists

We previously disclosed that 6-aryl benzoxazin-2-ones were PR modulators. In a continuation of this work we examined the SAR of new 6-arylamino benzoxazinones and found the targets 1-25, with an extra amino linker between the pendent 6-aryl groups and ben

NOVEL LONG-WORKING BETA-2-AGONISTS AND USE THEREOF AS MEDICAMENTS

The invention relates to compounds of formula (1), wherein groups X, Ra, Rb, R1, R1', R2, R2', R2'', R2''', V and n can have the meanings as cited in the claims and in

New long acting beta-2-agonists and their use as medicaments

The present invention relates to compounds of formula 1 wherein the groups X, Ra, Rb, R1, R1′, R2, R2′, R2″, R2′″, V and n may have the meanings given in the claims an