3,4-DICHLORO-[1,2]NAPHTHOQUINONE

Base Information

• Chemical Name: 3,4-DICHLORO-[1,2]NAPHTHOQUINONE
• CAS No.: 18398-36-2
• Molecular Formula: C10H4Cl2O2
• Molecular Weight: 227.047
• Hs Code.: 2914700090
• Mol file: 18398-36-2.mol

Synonyms:3,4-Dichloro-1,2-naphthoquinone;3,4-dichloro-1,2-naphthalenedione;1,2-Naphthalenedione, 3,4-dichloro-;BB_SC-2729;1,2-Naphthalenedione,3,4-dichloro;

Chemical Property of 3,4-DICHLORO-[1,2]NAPHTHOQUINONE

Chemical Property:

• Melting Point: 184°C
• Refractive Index: 1.5410 (estimate)
• Boiling Point: 325.12°C (rough estimate)
• PSA: 34.14000
• Density: 1.4057 (rough estimate)
• LogP: 2.59820

Purity/Quality:

99% ^*data from raw suppliers

3,4-DICHLORO-1,2-NAPHTHOQUINONE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Use Description: 3,4-Dichloro-[1,2]naphthoquinone is a chemical compound with varied applications across different fields. In the field of organic chemistry, it can serve as a valuable building block for the synthesis of complex organic molecules, making it important for the development of pharmaceuticals and agrochemicals. In the textile industry, 3,4-DICHLORO-[1,2]NAPHTHOQUINONE may find use as a dye and dye intermediate, contributing to the production of colored textiles and pigments. Additionally, in the realm of analytical chemistry, it can be employed as a reagent for analytical testing, aiding in the detection and quantification of specific compounds. Its versatility as a building block, dye component, and analytical reagent highlights its significance in advancing chemical research, textile production, and analytical science in various fields.

Technology Process of 3,4-DICHLORO-[1,2]NAPHTHOQUINONE

There total 12 articles about 3,4-DICHLORO-[1,2]NAPHTHOQUINONE 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:

→ 3,4-dichloro-[1,2]naphthoquinone (18398-36-2)

Guidance literature:

With acetyl chloride; at 100 ℃;

Reference yield:

1,3,4-trichloro-[2]naphthol (56961-40-1) → 3,4-dichloro-[1,2]naphthoquinone (18398-36-2)

Guidance literature:

With nitric acid; acetic acid;

Reference yield:

→ 3,4-dichloro-[1,2]naphthoquinone (18398-36-2)

Guidance literature:

With chlorine; acetic acid;

upstream raw materials:

1,3,4-trichloro-[2]naphthol

3,4-dichloro-1,2-naphthoquinone-1-oxime

acetyl chloride

1,2-naphthoquinone

Downstream raw materials:

3-chloro-4-(2-methyl-aziridin-1-yl)-[1,2]naphthoquinone

5,6-dihydronaphtho<1',2':4,5>imidazo<1,2-a>pyridine-5,6-dione

3-chloro-4-(2,2-dimethyl-aziridin-1-yl)-[1,2]naphthoquinone

2,2-dichloroindan-1,3-dione

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