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Key Documents

A62809

Sigma-Aldrich

3-Amino-4-methylbenzoic acid

99%

Synonym(s):

3-Amino-p-toluic acid

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About This Item

Linear Formula:
H2NC6H3(CH3)CO2H
CAS Number:
Molecular Weight:
151.16
Beilstein/REAXYS Number:
2082449
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

assay

99%

form

powder, crystals or chunks

reaction suitability

reaction type: solution phase peptide synthesis

color

white to purple

mp

164-168 °C (lit.)

application(s)

peptide synthesis

SMILES string

Cc1ccc(cc1N)C(O)=O

InChI

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

InChI key

XKFIFYROMAAUDL-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Weixiang Liu et al.
Carbohydrate polymers, 160, 97-105 (2017-01-25)
A novel type of O-carboxymethyl chitosan Schiff bases (O-CSPX) was synthesized via a condensation reaction. After the coordination reaction of cupric ions, Cu(II) complexes (O-CSPX-Cu) were achieved. The theoretical structure of O-CSPX-Cu calculated by Gaussian 09 reveals that the copper

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