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10-methoxy-6,7-dihydro-5H-pyrimido[5,4-c]carbazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88368-20-1

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88368-20-1 Usage

Chemical class

Hetrocyclic aromatic organic compound

Parent compound

Carbazole

Derivative

10-methoxy-6,7-dihydro-5H-pyrimido[5,4-c]carbazole

Methoxy group (CH3O-)

Attached at the 10th position

Dihydro group (H2)

Attached at the 6th and 7th positions

Core structure

Fused pyrimidine and carbazole rings

Potential applications

Biological and pharmaceutical (requiring further research and analysis)

Molecular complexity

Complex molecular structure

Fused rings

Pyrimidine and carbazole rings are fused together

Heteroatoms

Presence of nitrogen and oxygen atoms in the structure

Aromaticity

Due to the presence of fused aromatic rings

Reactivity

May undergo reactions typical of carbazole derivatives (e.g., electrophilic substitution, nucleophilic substitution)

NMR spectroscopy

To determine the structure and position of functional groups

Mass spectrometry

To confirm the molecular weight and composition

X-ray crystallography

To determine the three-dimensional structure of the compound

Elemental analysis

To determine the elemental composition of the compound

Synthesis

May involve chemical reactions such as cyclization, substitution, or reduction to form the desired compound

Stability

Requires investigation to determine stability under various conditions (e.g., temperature, pH, light exposure)

Solubility

May vary depending on the solvent used (e.g., polar or nonpolar solvents)

Purity

Requires purification techniques such as chromatography to obtain a pure sample for analysis and application

Safety and handling

Proper safety measures and handling procedures should be followed to minimize risks associated with the compound (e.g., use of gloves, eye protection, and proper disposal methods)

Check Digit Verification of cas no

The CAS Registry Mumber 88368-20-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,6 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88368-20:
(7*8)+(6*8)+(5*3)+(4*6)+(3*8)+(2*2)+(1*0)=171
171 % 10 = 1
So 88368-20-1 is a valid CAS Registry Number.

88368-20-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-methoxy-6,7-dihydro-5H-pyrimido[5,4-c]carbazole

1.2 Other means of identification

Product number -
Other names dihydro-6,7 methoxy-10 5H-pyrimidino<5,4-c>carbazole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88368-20-1 SDS

88368-20-1Downstream Products

88368-20-1Relevant academic research and scientific papers

Synthese de Dihydro-6,7 5H-pyrimidinocarbazoles et de 7H-Pyrimidinocarbazoles

Lancelot, Jean-Charles,Gazengel, Jean-Marie,Robba, Max

, p. 2652 - 2661 (2007/10/02)

The synthesis of 6,7-dihydro-5H-pyrimidinocarbazoles (3) was achived by cyclisation of 1,2,3,4-tetrahydrocarbazol-4-ones with triformamidomethane.The oxydation with potassium permanganate of 6,7-dihydro-5H-pyrimidinocarbazoles gave the 7H-pyrimidinocarbazoles (4).The reactions of the pyrimidinocarbazoles (4a) and (4e) with lithium organic compounds afforded 4-substituted derivatives (6).The structure of the derivatives was determined by (1)H-NMR and Overhauser effect.Keywords - 1,2,3,4-tetrahydrocarbazol-4-one; 6,7-dihydro-5H-pyrimidinocarbazole; 7H-pyrimidinocarbazole; (1)H-NMR; Overhauser effect

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