2-Amino-6-methylbenzoic acid, 98%

Name: 2-Amino-6-methylbenzoic acid, 98%
SKU: A15187.22

CAS: 4389-50-8 | C8H8NO2 | 150.16 g/mol

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数量:

5 g

25 g

100 g

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製品番号（カタログ番号） A15187.22

または、製品番号A15187-22

価格（JPY）

数量:

100 g

一括またはカスタム形式をリクエストする

化学物質識別子

CAS4389-50-8

IUPAC Name2-amino-6-methylbenzoate

Molecular FormulaC8H8NO2

InChI KeyXHYVBIXKORFHFM-UHFFFAOYSA-M

SMILESCC1=CC=CC(N)=C1C([O-])=O

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仕様

スペックシート

Appearance (Color)Pale cream to cream to pale brown

FormPowder

Assay (Aqueous acid-base Titration)≥97.5 to ≤102.5%

Assay (Silylated GC)≥97.5%

2-Amino-6-methylbenzoic acid reacts with cyanogen bromide to prepare 2-amino-5-methyl-benzo[d][1,3]oxazin-4-one.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2-Amino-6-methylbenzoic acid reacts with cyanogen bromide to prepare 2-amino-5-methyl-benzo[d][1,3]oxazin-4-one.

Solubility
Soluble in methanol.

Notes
Incompatible with strong oxidizing agents and strong acids.

RUO – Research Use Only

General References:

Ma, C.; Gong, G.; Liu, Z.; Ma, A.; Chen, Z. Stimulatory effects of tea supplements on the propagation of Lactobacillus casei in milk. Int. Dairy. J. 2015, 43, 1-6.
Pearson, A. J.; Panda, S. N-Prolinylanthranilic acid derivatives as bifunctional organocatalysts for asymmetric aldol reactions. Tetrahedron 2011, 67 (22), 3969-3975.
Wang, D.; Lin, H.; Cao, R.; Yang, S.; Chen, Q.; Hao, G.; Yang, W.; Yang, G. Synthesis and Herbicidal Evaluation of Triketone-Containing Quinazoline-2,4-diones. J. Agric. Food Chem. 2014, 62 (49), 11786-11796.