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1-Naphthalenamine, 3-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

3229-86-5

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3229-86-5 Usage

Usage

Intermediate in the synthesis of various organic compounds and dyes

Physical description

Pale yellow solid

Solubility

Soluble in organic solvents, limited solubility in water

Chemical classification

Nitroaniline derivative

Health hazards

Can cause skin, eye, and respiratory irritation; toxic if ingested or inhaled in large amounts

Check Digit Verification of cas no

The CAS Registry Mumber 3229-86-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,2 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3229-86:
(6*3)+(5*2)+(4*2)+(3*9)+(2*8)+(1*6)=85
85 % 10 = 5
So 3229-86-5 is a valid CAS Registry Number.

3229-86-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-nitronaphthalen-1-amine

1.2 Other means of identification

Product number -
Other names 3-Nitro-1-naphthylamine

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:3229-86-5 SDS

3229-86-5Upstream product

3229-86-5Relevant academic research and scientific papers

Studies directed towards nonyl acridine orange analogues having the potential to act as FRET donors with the PDT drug Pc 4

Zhang, Ping,Yang, Yang,Liu, Yun,Rodriguez, Myriam E.,Kenney, Malcolm E.

, p. 29391 - 29403 (2016)

A group of nonyl acridine orange analogues (NAO) was prepared which were designed to have the potential of possessing visible bands allowing them to act in cells as fluorescence resonance energy transfer (FRET) donors with the photodynamic therapy drug Pc 4. The existence of Pc 4-FRET with the analogues of NAO in MCF-7c3 cells was probed. The results suggest that NAO analogues giving strong FRET with Pc 4 in cells can be found.

INDO- AND BENZINDOCYANINE DYES WITH FLUORINE-CONTAINING SUBSTITUENTS

Pazenok, S. V.,Kondratenko, N. V.,Popov, V. I.,Troitskaya, V. I.,Il'chenko, A. Ya.,et al.

, p. 1182 - 1187 (2007/10/02)

Syntheses are reported for 2,3,3-trimethyl-3H-indoles and 1,1,2-trimethyl-1H-benzindoles with fluorine-containing substituents (CF3, SCF3, and SO2CF3) at C-5 and for carbocyanine, merocyanine, and styryl dye derivatives of these indoles.The fluorine-containing substituents studied produce a bathochromic effect in the styryl dyes, hypsochromic effect in the merocyanine dyes, and, as a rule, a hypsochromic effect in the carbocyanine dyes.

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