| Identification | More | [Name]
2-Amino-6-chlorobenzoic acid | [CAS]
2148-56-3 | [Synonyms]
2-AMINO-6-CHLOROBENZOIC ACID
6-AMINO-2-CHLOROBENZOIC ACID
6-CHLOROANTHRANILIC ACID
RARECHEM AL BO 1514
TIMTEC-BB SBB001735
Benzoic acid, 2-amino-6-chloro-
6-Chloro-2-aminobenzoic acid
2-choro-6-Aminobenzoic Acid
BENZOIC ACID, 2-AMINO-6-CHLORO-(9CI)
2-AMINO-6-CHLOROBENZOIC ACID(6-CHLOROANTHRANILIC ACID)
6-AMINO-2-CHLOROBENZOC ACID
6-Chloroanthranilic acid (COOH=1)
2-AMINO-6-CHLOROBENZOIC ACID 98% | [EINECS(EC#)]
218-416-8 | [Molecular Formula]
C7H6ClNO2 | [MDL Number]
MFCD00051530 | [Molecular Weight]
171.58 | [MOL File]
2148-56-3.mol |
| Chemical Properties | Back Directory | [Appearance]
white to light yellow crystal powder | [Melting point ]
158-160 °C (lit.) | [Boiling point ]
250°C (rough estimate) | [density ]
1.3246 (rough estimate) | [refractive index ]
1.5560 (estimate) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [form ]
Crystalline Powder | [pka]
0.97±0.10(Predicted) | [color ]
Light yellow to beige | [Water Solubility ]
Very soluble in water. Soluble in methanol. | [BRN ]
2804041 | [InChI]
InChI=1S/C7H6ClNO2/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3H,9H2,(H,10,11) | [InChIKey]
SZCPTRGBOVXVCA-UHFFFAOYSA-N | [SMILES]
C(O)(=O)C1=C(Cl)C=CC=C1N | [CAS DataBase Reference]
2148-56-3(CAS DataBase Reference) | [NIST Chemistry Reference]
2-Amino-6-chlorobenzoic acid(2148-56-3) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HS Code ]
29224999 |
| Hazard Information | Back Directory | [Chemical Properties]
white to light yellow crystal powder | [Uses]
2-Amino-6-chlorobenzoic acid is used as intermediate for medicine. | [Application]
The tricyclohexyltin 2-amino-6-chlorobenzoate was synthesized by the reaction of the tricyclohexyltin hydroxide with the 2-amino-6-chlorobenzoic acid. | [Preparation]
A, in the reaction vessel being provided with agitator, thermometer, reflux condenser, Dropping funnel, add cerium chloride 0.16mol, 4-hydroxy 3-methoxybenzene ethanol solution 0.19mol, Klorvess Liquid 400-500ml, control mixing speed and exist 160-190rpm, rising solution temperature, to 60-65°C, is slowly added to 2-chloro-6-nitrobenzoyl acid solution 0.13mol, sulfurous acid Hydrogen potassium solution 200ml, raises mixing speed to 260-310rpm, back flow reaction 5-7h；
B, reduction solution temperature, to 15-19°C, separate out solid, filter, and add diammonium hydrogen citrate solution 150-in filtrate 180ml, concentrating under reduced pressure, separate out solid, filter, dehydrant is dehydrated, brine, and pyridine solution washs, ethyl acetate solution Middle recrystallization, obtains crystal 2-amino-6-chlorobenzoic acid (C7H6ClNO2). | [reaction suitability]
reaction type: solution phase peptide synthesis | [Synthesis]
In a 250 mL round-bottomed flask, 5 g (32.77 mmol, 1.0 eq.) of 2-amino-6-chlorobenzonitrile was dissolved in 50 mL of a 30% aqueous potassium hydroxide (KOH) solution, followed by the addition of 3 mL of hydrogen peroxide (H2O2). The mixture was reacted under reflux conditions overnight. Upon completion of the reaction, the reaction mixture was washed sequentially with ether and dichloromethane each, followed by acidification. The acidified mixture was extracted with dichloromethane and ethyl acetate, and after separating the organic layer, the organic layer was washed with saturated brine. The organic layer was dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure to give 5.31 g (30.95 mmol, 94% yield) of 2-amino-6-chlorobenzoic acid as an orange solid. | [References]
[1] Patent: KR2017/74380, 2017, A. Location in patent: Paragraph 0175-0178
[2] Patent: US2018/105527, 2018, A1. Location in patent: Paragraph 0439-0441 |
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