tetramethyl 9H-carbazole-1,2,3,4-tetracarboxylate

Base Information

Chemical Name:tetramethyl 9H-carbazole-1,2,3,4-tetracarboxylate
CAS No.:37914-34-4
Molecular Formula:C₂₀H₁₇NO₈
Molecular Weight:399.357
Hs Code.:

Synonyms:

Suppliers and Price of tetramethyl 9H-carbazole-1,2,3,4-tetracarboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of tetramethyl 9H-carbazole-1,2,3,4-tetracarboxylate

Chemical Property:

Vapor Pressure:1.08E-10mmHg at 25°C

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tetramethyl 9H-carbazole-1,2,3,4-tetracarboxylate

There total 4 articles about tetramethyl 9H-carbazole-1,2,3,4-tetracarboxylate 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: 1.1%

: 120-72-9
indole

: 762-42-5
dimethyl acetylenedicarboxylate

: 37914-34-4
carbazole-1,2,3,4-tetracarboxylic acid tetramethyl ester

: 37914-36-6
Trimethyl 6-oxo-5H-phenanthridine-2,3,4-tricarboxylate

: 6267-88-5
Indol-3-fumarsaeuredimethylester

: 9-((Z)-1,2-Bis-methoxycarbonyl-vinyl)-9H-carbazole-2,3-dicarboxylic acid dimethyl ester

Guidance literature:: In dichloromethane; for 24h; under 10000 Torr;

Reference yield:

: 101606-93-3
3,4-dicyano-carbazole-1,2-dicarboxylic acid dimethyl ester

: 37914-34-4
carbazole-1,2,3,4-tetracarboxylic acid tetramethyl ester

Guidance literature:: With potassium hydroxide; Behandeln des nach Ansaeuern mit wss. HCl erhaltenen Reaktionsgemisches mit Diazomethan in Aether;
DOI:10.1021/ja01531a039