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进行环缩合以形成，例如，喹喔啉和苯并咪唑。 Undergoes cyclocondensations to form, for example, quinoxalines and benzimidazoles. 3,4-Diaminobenzoic acid can be used to prepare: · Schiff base derivatives by reacting with substituted aldehydes and their corresponding metal complexes. · Poly(2,5-benzimidazole) (ABPBI) polymer by reacting with methanesulfonic acid and P2O5. · Pt-based Schiff base complexes applicable in H2O splitting reactions. 3,4-Diaminobenzoic acid undergoes cyclocondensations to form, for example, quinoxalines and benzimidazoles Undergoes cyclocondensations to form, for example, quinoxalines and benzimidazoles. 3,4-Diaminobenzoic acid can be used to prepare: · Schiff base derivatives by reacting with substituted aldehydes and their corresponding metal complexes. · Poly(2,5-benzimidazole) (ABPBI) polymer by reacting with methanesulfonic acid and P2O5. · Pt-based Schiff base complexes applicable in H2O splitting reactions. 3,4-Diaminobenzoic acid undergoes cyclocondensations to form, for example, quinoxalines and benzimidazoles

Specs ⸢ View details ⸥

Chinese name

3,4-二氨基苯甲酸

English name

3,4-Diaminobenzoic acid

Chinese alias

3,4-二氨基安息香酸

English alias

CAS number

619-05-6

molecular formula

(H2N)2C6H3CO2H

molecular weight

152.15 g/mol

Exact mass

≥99%

PSA

89.300 Å²

Logp

0.200

Technical Documents

「No technical documents」

「No upstream and downstream information yet」

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Research chemical ≥98. 0%; 100mg

Name: Research chemical ≥98. 0%; 100mg
Brand: TMstandard
SKU: 715265-100mg

Research chemical ≥98. 0%; 100mg; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: ≥98. 0%; 100mg.

item number：715265-100mg

Product model：100mg

level： ≥98. 0%; 100mg

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Research chemical ≥98. 0%; 100mg

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