ChemicalBook--->CAS DataBase List--->2486-75-1

2486-75-1

2486-75-1 Structure

2486-75-1 Structure
IdentificationMore
[Name]

4-Amino-2-methylbenzoic acid
[CAS]

2486-75-1
[Synonyms]

2-METHYL-4-AMINO-BENZOIC ACID
4-AMINO-2-METHYLBENZOIC ACID
4-Amino-2-methybenzoic acid
Benzoic acid, 4-amino-2-methyl-(9CI)
4-Amino-o-toluic
[EINECS(EC#)]

200-297-9
[Molecular Formula]

C8H9NO2
[MDL Number]

MFCD06656133
[Molecular Weight]

151.16
[MOL File]

2486-75-1.mol
Chemical PropertiesBack Directory
[Melting point ]

160-165 °C
[Boiling point ]

339.5±30.0 °C(Predicted)
[density ]

1.254±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

soluble in Methanol
[form ]

Solid
[pka]

4.86±0.25(Predicted)
[color ]

Light orange to Yellow to Green
[Major Application]

peptide synthesis
[InChI]

InChI=1S/C8H9NO2/c1-5-4-6(9)2-3-7(5)8(10)11/h2-4H,9H2,1H3,(H,10,11)
[InChIKey]

XRSQZFJLEPBPOZ-UHFFFAOYSA-N
[SMILES]

C(O)(=O)C1=CC=C(N)C=C1C
[CAS DataBase Reference]

2486-75-1(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P264-P270-P301+P312-P501
[Hazard Codes ]

Xn
[Risk Statements ]

R22:Harmful if swallowed.
[Safety Statements ]

26
[WGK Germany ]

3
[HS Code ]

29224999
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Hazard InformationBack Directory
[Chemical Properties]

White powder
[Uses]

peptide synthesis
[reaction suitability]

reaction type: solution phase peptide synthesis
[Synthesis]

2-Methyl-4-nitrobenzoic acid

1975-51-5

4-Amino-2-methylbenzoic acid

2486-75-1

GENERAL STEPS: Prior to each experiment, the tubular reaction apparatus was equilibrated by pumping solvent for 30 min at 16 bar hydrogen pressure (see Fig. 4). An Omnifit reaction cartridge (20.0 mm outer diameter, 15.0 mm inner diameter) containing 1 g Pd/C catalyst was used. To prevent overpressurization of the system in case of blockage, the upper pressure of the Knauer pump was set to 25 bar. with the injection ring disconnected from the flow line, the injection ring was opened and manually injected with 3.6 mL of a 0.076 M ethanol solution of 2-methyl-4-nitrobenzoic acid (excess feedstock solution in the ring was recovered for reuse). The injection ring was then closed and plugged into the flow stream. Collect the product at the outlet of the system downstream of the backpressure regulator for 120 min. The solvent is removed by reduced pressure distillation (first using a rotary evaporator and then a secondary rotary vane pump) to give 4-amino-2-methylbenzoic acid.

[References]

[1] Tetrahedron, 2018, vol. 74, # 47, p. 6795 - 6803
[2] Chemische Berichte, 1884, vol. 17, p. 161
[3] Patent: US2012/46467, 2012, A1. Location in patent: Page/Page column 26
Spectrum DetailBack Directory
[Spectrum Detail]

4-Amino-2-methylbenzoic acid(2486-75-1)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

2486-75-1(sigmaaldrich)
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