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Benzo[c]phenanthren-2-amine is a chemical compound with the molecular formula C17H13N and the chemical structure consisting of a benzo[c]phenanthrene core with an amine group attached at the 2-position. Benzo[c]phenanthren-2-amine is a polycyclic aromatic amine, which is a type of organic compound with multiple fused aromatic rings and an amino group. Benzo[c]phenanthren-2-amine is known for its potential mutagenicity and carcinogenicity, as it can form DNA adducts and cause genetic mutations. It is also a structural analog of the more well-known carcinogen, benzo[a]pyrene. Due to its hazardous properties, it is important to handle Benzo[c]phenanthren-2-amine with caution and to study its effects on human health and the environment.

4235-06-7

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4235-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4235-06-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,3 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4235-06:
(6*4)+(5*2)+(4*3)+(3*5)+(2*0)+(1*6)=67
67 % 10 = 7
So 4235-06-7 is a valid CAS Registry Number.

4235-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzo[c]phenanthren-2-amine

1.2 Other means of identification

Product number -
Other names 2-Amino-benzo<c>phenanthren

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:4235-06-7 SDS

4235-06-7Downstream Products

4235-06-7Relevant academic research and scientific papers

Circularly Polarized Fluorescent Helicene-Boranils: Synthesis, Photophysical and Chiroptical Properties

, p. 7959 - 7967 (2021)

Mono- and di-boranil-substituted helicenes were prepared by BF2-borylation of the corresponding anils, readily synthesized by condensation of 2-amino- and 2,15-diamino-helicenes with 4-(diethylamino)salicylaldehyde. After enantiomeric resolutio

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