Aluminum phthalocyanine hydroxide

Base Information

• Chemical Name: Aluminum phthalocyanine hydroxide
• CAS No.: 15554-15-1
• Molecular Formula: C₃₂H₁₇AlN₈O
• Molecular Weight: 556.522
• European Community (EC) Number: 627-305-7
• Mol file: 15554-15-1.mol

Synonyms:Aluminum phthalocyanine hydroxide;hydroxyaluminium phthalocyanine;AKOS015911944;Aluminum phthalocyanine hydroxide, Dye content 85 %

Chemical Property of Aluminum phthalocyanine hydroxide

Chemical Property:

• PSA: 114.71000
• LogP: 8.98300
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 557.1418956
• Heavy Atom Count: 42
• Complexity: 1160

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C3=NC4=C5C=CC=CC5=C6N4[Al]N7C(=NC2=N3)C8=CC=CC=C8C7=NC9=NC(=N6)C1=CC=CC=C19.O

Technology Process of Aluminum phthalocyanine hydroxide

There total 12 articles about Aluminum phthalocyanine hydroxide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 93.0%

C15H17FN2O3 (143655-70-3) → 2-Acetylamino-8-amino-6-fluoro-5-methyl-1-tetralone (182182-31-6)

Guidance literature:

With hydrogenchloride; In methanol; at 60 ℃; for 0.5h; Inert atmosphere;

Reference yield: 77.0%

diethyl thioglycolate (925-47-3) + oxalic acid diethyl ester (95-92-1) → 3,4-dihydroxythiophene-2,5-dicarboxylic acid diethyl ester (1822-66-8)

Guidance literature:

diethyl thioglycolate; oxalic acid diethyl ester; With ethanol; sodium; at 0 - 25 ℃; for 25h; Inert atmosphere;

With hydrogenchloride; In water; pH=2; Inert atmosphere;

DOI:10.1039/c4ra13060j

Reference yield:

chloroaluminum phthalocyanine (14154-42-8,62905-77-5) + water (7732-18-5) → hydroxyaluminum(III) phthalocyanine (15554-15-1,62905-64-0)

Guidance literature:

With sodium hydroxide; In acetone; at 50 ℃; for 4h;

upstream raw materials:

C₁₅H₁₇FN₂O₃

3-fluoro-4-methyl-phenylamine

N-(3-fluoro-4-methylphenyl)acetamide

C₉H₉BrFNO

Downstream raw materials:

fluoro-aluminium phthalocyanine

aluminum phthalocyanine benzoate

aluminum phthalocyanine propionate

aluminum phthalocyanine acetate

Refernces

• 1、 -. "Intermediate for synthesizing camptothecin derivative as well as preparation method and application thereof". . . Retrieved 2020/08/09.
• 2、 -. "Aminothiophene sulfonic acid ester". Paragraph 0059; 0061. . Retrieved 2018/02/28.