CAS 102-51-2

4-Methoxy-o-phenylenediamine

Description:

4-Methoxy-o-phenylenediamine, with the CAS number 102-51-2, is an organic compound characterized by the presence of two amino groups (-NH2) and a methoxy group (-OCH3) attached to a benzene ring. This compound is a derivative of phenylenediamine, specifically positioned with the methoxy group at the para position relative to one of the amino groups. It typically appears as a solid and is soluble in organic solvents. The presence of the methoxy group enhances its electron-donating properties, which can influence its reactivity and interactions in various chemical processes. 4-Methoxy-o-phenylenediamine is often utilized in the synthesis of dyes, pigments, and other organic compounds due to its ability to participate in electrophilic aromatic substitution reactions. Additionally, it may have applications in the field of polymer chemistry and as an intermediate in the production of various chemical products. Safety precautions should be observed when handling this compound, as it may pose health risks upon exposure.

Formula: C₇H₁₀N₂O

InChI: InChI=1/C7H10N2O/c1-10-5-2-3-6(8)7(9)4-5/h2-4H,8-9H2,1H3

InChI key: InChIKey=AGAHETWGCFCMDK-UHFFFAOYSA-N

SMILES: O(C)C1=CC(N)=C(N)C=C1

Synonyms:

• 1,2-Benzenediamine, 4-methoxy-
• 1,2-Diamino-4-methoxybenzene
• 2-Amino-4-methoxyaniline
• 3,4-Diamino Anisole
• 3,4-Diaminoanisole
• 4-Methoxy-1,2-benzenediamine
• 4-Methoxy-1,2-diaminobenzene
• 4-Methoxy-1,2-phenylenediamine
• 4-Methoxy-2-aminoaniline
• 4-Methoxybenzene-1,2-Diamine
• Methoxyophenylenediamine
• o-Phenylenediamine, 4-methoxy-
• p-Methoxy-o-phenylenediamine
• 4-METHOXY-BENZENE-1,2-DIAMINE
• 3,4-Diaminoanisidine
• 4-methoxy-o-phenylenediamin
• 4-methoxy-2-benzenediamine
• 2-amino-4-methoxyphenylamine
• 4-METHOXY-O-PHENYLENEDIAMINE
• 4-Methoxyphenylenediamine, 98%

1,2-Benzenediamine, 4-methoxy-

CAS: 102-51-2

Formula: C₇H₁₀N₂O

Purity: 97%

Color and Shape: Solid

Molecular weight: 138.1671

Ref: IN-DA00068K

4-Methoxybenzene-1,2-diamine

CAS: 102-51-2

Formula: C₇H₁₀N₂O

Purity: >98.0%(GC)(T)

Color and Shape: White to Amber powder to crystal

Molecular weight: 138.17

Ref: 3B-M2882

4-Methoxybenzene-1,2-diamine

CAS: 102-51-2

4-Methoxybenzene-1,2-diamine

Formula: C₇H₁₀N₂O

Purity: 97%

Color and Shape: faint grey to grey fused solid

Molecular weight: 138.17g/mol

Ref: 54-OR21113

3,4-Diaminoanisole

CAS: 102-51-2

Formula: C₇H₁₀N₂O

Molecular weight: 138.17

Ref: 4Z-B-139078

3,4-Diaminoanisole

CAS: 102-51-2

Applications 3,4-Diaminoanisole (cas# 102-51-2) is a compound useful in organic synthesis.

Formula: C₇H₁₀N₂O

Color and Shape: Neat

Molecular weight: 138.17

Ref: TR-D416125

3,4-Diaminoanisole

CAS: 102-51-2

Formula: C₇H₁₀N₂O

Purity: 97%

Color and Shape: Crystalline Powder

Molecular weight: 138.17

Ref: 10-F092184

4-methoxybenzene-1,2-diamine

CAS: 102-51-2

4-Methoxybenzene-1,2-diamine is a chemical intermediate that is used in the production of quinoxalines. It is an intramolecular hydrogen acceptor and undergoes an acid-catalyzed reaction with glyoxal to form 4-methoxybenzene-1,2-diol. This reaction mechanism has been observed in urine samples. The skeleton of 4-methoxybenzene-1,2-diamine consists of a phenyl group and a hydroxyl group. The cationic polymerization of 4-methoxybenzene-1,2-diamine can be achieved by adding tyrosinase as a catalyst. This chemical has been shown to have diphenolase activity. Chemical ionization (CI) is one way to measure the quantity of this compound in urine samples because it reacts with hydrochloric acid to produce hydrogen chloride ions.

Formula: C₇H₁₀N₂O

Purity: Min. 95%

Molecular weight: 138.17 g/mol

Ref: 3D-FM21476