5043-81-2

Basic information

• Product Name: Methyl 3-amino-5-chloro-2-hydroxybenzoate
• Synonyms: 3-AMINO-5-CHLORO-2-HYDROXYBENZOIC ACID METHYL ESTER;methyl 3-amino-5-chloro-2-hydroxybenzoate;Methyl 3-amino-5-chlorosalicylate;3-AMINO-5-CHLORO-2-HYDROXYBENZOIC ACID ME ESTER;3-amino-5-chloro-2-hydroxybenzoate;SALICYLICACID,3-AMINO-5-CHLORO-,METHYLESTER(7CI,8CI);3-Amino-5-chloro-salicylic Acid Methyl Ester;methyl 3-amino-5-chloro-2-hydroxybenzoate hydrochloride
• CAS NO: 5043-81-2
• Molecular Formula: C₈H₈ClNO₃
• Molecular Weight: 201.61
• Product Categories: Benzoic acid;Amines;Aromatics;Intermediates
• Mol File: 5043-81-2.mol

Chemical Properties

• Melting Point: 71-73°C
• Boiling Point: 322°C at 760 mmHg
• Flash Point: 148.5°C
• Appearance: /
• Density: 1.44g/cm³
• Vapor Pressure: 0.000153mmHg at 25°C
• Refractive Index: 1.617
• Storage Temp.: -20°C Freezer
• Solubility: DMSO (Slightly), Methanol (Slightly)
• PKA: 9.11±0.23(Predicted)
• CAS DataBase Reference: Methyl 3-amino-5-chloro-2-hydroxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 3-amino-5-chloro-2-hydroxybenzoate(5043-81-2)
• EPA Substance Registry System: Methyl 3-amino-5-chloro-2-hydroxybenzoate(5043-81-2)

Safety Data

• Hazardous Substances Data: 5043-81-2(Hazardous Substances Data)

Usage

Chemical Properties

Light Brown Solid

InChI:InChI=1/C8H8ClNO3/c1-13-8(12)5-2-4(9)3-6(10)7(5)11/h2-3,11H,10H2,1H3

Upstream product

• 4068-78-4 methyl 5-chloro-2-hydroxybenzoate 
• 5043-79-8 5-chloro-2-hydroxy-3-nitrobenzoic acid methyl ester 

Downstream Products

• 123040-16-4 Azasetron hydrochloride 
• 141761-83-3 6-chloro-4-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-8-carboxylic acid methyl ester 
• 873862-55-6 methyl 3-acetylamino-5-chlorosalicylate 
• 141762-14-3 6-Chloro-3-oxo-4-phenethyl-3,4-dihydro-2H-benzo[1,4]oxazine-8-carboxylic acid (1-aza-bicyclo[2.2.2]oct-3-yl)-amide 
• 141762-13-2 4-Benzyl-6-chloro-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-8-carboxylic acid (1-aza-bicyclo[2.2.2]oct-3-yl)-amide 
• 141762-06-3 6-Chloro-4-methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-8-carboxylic acid (1-benzyl-piperidin-4-yl)-amide 
• 141762-05-2 6-Chloro-4-methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-8-carboxylic acid (1-benzyl-piperidin-3-yl)-amide 
• 123040-69-7 azasetron 
• 141761-94-6 6-Chloro-3-oxo-4-phenethyl-3,4-dihydro-2H-benzo[1,4]oxazine-8-carboxylic acid methyl ester 
• 141762-01-8 6-Chloro-3-oxo-4-phenethyl-3,4-dihydro-2H-benzo[1,4]oxazine-8-carboxylic acid 
• 141761-93-5 4-Benzyl-6-chloro-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-8-carboxylic acid methyl ester 
• 141762-00-7 4-Benzyl-6-chloro-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-8-carboxylic acid 
• 123040-50-6 6-chloro-3,4-dihydro-4-methyl-3-oxo-2H-1,4-benzoxazine-8-carboxylic acid chloride 
• 123040-79-9 6-chloro-3,4-dihydro-4-methyl-3-oxo-2H-1,4-benzoxazine-8-carboxylic acid 

Relevant articles and documents

Synthesis method of azasetron hydrochloride intermediate methyl 3-amino-5-chloro-2-hydroxybenzoate

The invention discloses a synthesis method of azasetron hydrochloride intermediate methyl 3-amino-5-chloro-2-hydroxybenzoate, which comprises the following steps: (1) dissolving methyl 5-chloro-2-hydroxy-3-nitrobenzoate in ethanol, adding stannous chlorid

Novel preparation method of azasetron hydrochloride

The invention provides a novel preparation method of azasetron hydrochloride, belonging to the technical field of medicine synthesis. According to the method, methyl 5-chlorosalicylate is used as a raw material; after acetic anhydride nitrification and stannous chloride reduction at room temperature, dimethyl carbonate is used as a methylation reagent, and an intermediate V (6-chloro-4-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-8-carboxylic acid methyl ester) is synthesized by adopting a one-pot method; the intermediate V is hydrolyzed to obtain 6-chloro-4-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-8-formic acid (VI); and the compound reacts with free 3-aminoquinuclidine dihydrochloride for 1 h under the catalysis of TBTU to form a salt so as to obtain I (azasetron hydrochloride). According to the method, the yield of each step is high; aftertreatment is simple; the reaction time of each step is short; conditions are mild; low-toxicity environment-friendly reagents are adopted; energy consumption is reduced; cost is saved; and industrial production is better facilitated.

AMINO PYRAZOLONE DERIVATIVE HAVING CONDENSED RING STRUCTURE

PROBLEM TO BE SOLVED: To provide a compound that has excellent inhibitory action on ATPase activity of TIP48/TIP49 complex and is therefore useful for the treatment of tumor, or a pharmacologically acceptable salt thereof. SOLUTION: The present invention provides a compound having a structure represented by general formula (I), its pharmacologically acceptable salt, or a pharmaceutical composition comprising the compound (where R3, R4, R5, R6, R7, W, X, Y, and Z are as defined in the specifications). SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

BENZO-FUSED HETEROCYCLIC DERIVATIVES USEFUL AS AGONISTS OF GPR120

The present invention is directed to benzo-fused heterocyclic derivatives, pharmaceutical compositions containing them and their use in the treatment of disorders and conditions modulated by GPR120. More particularly, the compounds of the present invention are agonists of GPR120, useful in the treatment of, such as for example, Type II diabetes mellitus.

CONDENSED BENZAMIDE COMPOUNDS AND INHIBITORS OF VANILLOID RECEPTOR SUBTYPE 1 (VR1) ACTIVITY

To provide a compound having an excellent inhibitory effect on vanilloid receptor subtype 1 (VR1) activity which is effective in treating diseases to which the vanilloid receptor subtype 1 (VR1) activity is involved, such as pain, acute pain, chronic pain

Synthesis and pharmacology of 3,4-dihydro-3-oxo-1,4-benzoxazine-8-carboxamide derivatives, a new class of potent serotonin-3 (5-HT3) receptor antagonists

A series of 3,4-dihydro-3-oxo-1,4-benzoxazine-8-carboxamide derivatives was synthesized and evaluated for serotonin-3 (5-HT3) receptor antagonistic activity assessed by their ability to antagonize the von Bezold-Jarish (BJ) effect in rats. Derivatives bearing 1-azabicyclo[2.2.2]oct-3-yl moiety as a basic function attached to the carboxamide at position 8 showed more potent antagonistic activity than those bearing the other three basic moieties. Structure activity relationships of this series showed that methyl and chloro groups were more effective as substituents at positions 4 and 6, respectively. The representative compound 15 (Y-25130) in this series showed potent antagonistic activity on the BJ effect (ED50 = 1.3 μg/kg i.v.), high affinity for 5-HT3 receptor (K(i) = 2.9 nM) and complete protection against cisplatin-induced emesis in dogs at a dose of 0.1 mg/kg i.v.