40484-36-4

Basic information

• Product Name: 6-(CHLOROMETHYL)PHENANTHRIDINE
• Synonyms: 6-(Chloromethyl)phenanthridine;NSC 8011
• CAS NO: 40484-36-4
• Molecular Formula: C₁₄H₁₀ClN
• Molecular Weight: 227.6889
• Mol File: 40484-36-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 394.2 °C at 760 mmHg
• Flash Point: 224.5 °C
• Appearance: /
• Density: 1.274 g/cm³
• Vapor Pressure: 4.56E-06mmHg at 25°C
• Refractive Index: 1.71
• CAS DataBase Reference: 6-(CHLOROMETHYL)PHENANTHRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(CHLOROMETHYL)PHENANTHRIDINE(40484-36-4)
• EPA Substance Registry System: 6-(CHLOROMETHYL)PHENANTHRIDINE(40484-36-4)

Safety Data

• Hazardous Substances Data: 40484-36-4(Hazardous Substances Data)

Usage

General Description

6-(Chloromethyl)phenanthridine is a chemical compound with the formula C18H13ClN. It is a member of the phenanthridine family, which are aromatic nitrogen-containing heterocycles. This particular compound contains a chloromethyl group attached to the phenanthridine ring, giving it unique chemical properties. It can serve as a building block for the synthesis of various organic compounds and may have applications in the pharmaceutical, agrochemical, and material science industries. However, it is important to handle this chemical with care due to its potential hazards and toxicity.

InChI:InChI=1/C14H10ClN/c15-9-14-12-7-2-1-5-10(12)11-6-3-4-8-13(11)16-14/h1-8H,9H2

Upstream product

• 128-09-6 N-chloro-succinimide 
• 3955-65-5 6-methylphenanthridine 
• 90-41-5 2-phenylaniline 
• 23088-28-0 N-([1,1'-biphenyl]-2-yl)-2-chloroacetamide 

Downstream Products

• 115173-64-3 N,N-bis-phenanthridin-6-ylmethyl-toluene-4-sulfonamide 
• 1015-89-0 phenanthridin-6-ol 
• 113518-45-9 6-(p-tosylamidomethyl)phenanthridine 
• 97511-51-8 2-tosyl-1,2,3,12b-tetrahydroimidazol<1,5-f>phenanthridine 
• 113518-44-8 C₂₂H₁₉⁽²⁾HN₂O₂S 
• 1015-89-0 6(5H)-phenanthridinone 
• 1271731-46-4 4-[(bis(6-phenanthridinylmethyl)amino)methyl]benzoic acid methyl ester 
• 1271731-41-9 4-[bis(6-phenanthridinylmethyl)aminomethyl]benzoic acid 
• 17613-40-0 bromo-6 phenanthridine 
• 115173-62-1 N-[2-(1,3-Dimethyl-6-methylamino-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl)-1-phenanthridin-6-yl-ethyl]-4-methyl-benzenesulfonamide 
• 115173-58-5 C₂₁H₁₉⁽²⁾HN₂O₂S 
• 115173-59-6 4-Methyl-N-(5-methyl-5,6-dihydro-phenanthridin-6-ylmethyl)-benzenesulfonamide 
• 97511-52-9 6-(p-tolylamidomethyl)-5,6-dihydrophenanthridine 
• 146174-68-7 4-t-butylcyclohexyl 6-phenanthridinylmethyl ether 

Relevant articles and documents

Controlling the isomerization rate of an azo-BF2 switch using aggregation

A novel visible-light activated azo-BF2 switch possessing a phenanthridinyl π-system has been synthesized, and its switching properties have been characterized as a function of concentration. The switch self-aggregates through π-π interactions, and the degree of aggregation modulates the Z → E thermal isomerization rate. This property allows for the active tuning of the thermal relaxation half-life of the same switch from seconds to days.

SYNTHESE DANS LA SERIE DES PHENANTHRIDINES. IV. PREPARATION DE NOUVEAUX RADIOPROTECTEURS A MOTIF PHENANTHRIDINE

New phenanthridines substituted in the 6-position by a β-aminoethylthiol chain have been synthesized.These new products are easily obtained from 6-methylphenanthridine by a Mannich reaction or from 6-bromophenanthridine by substitution.From the 6-carboxaldehydophenanthridine and the β-aminoethylthiol, the corresponding thiazolidine or imine are obtained.These compounds are likely to be new radioprotectors.