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3,7-Diaminodibenzofuran is an organic compound characterized by its molecular formula C8H8N2O and a molar mass of 148.16 g/mol. It is a derivative of dibenzofuran, featuring two amino groups attached at the 3 and 7 positions of the dibenzofuran ring. This chemical is known for its potential applications in the synthesis of various compounds, including dyes and polymers, due to its reactive amino groups. It is also recognized for its role as an intermediate in the production of certain pharmaceuticals. The compound is typically synthesized through chemical reactions and is handled with care due to its potential reactivity and the need to adhere to safety protocols.

5896-30-0

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5896-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5896-30-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,9 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5896-30:
(6*5)+(5*8)+(4*9)+(3*6)+(2*3)+(1*0)=130
130 % 10 = 0
So 5896-30-0 is a valid CAS Registry Number.

5896-30-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzofuran,1-benzofuran-3,7-diamine

1.2 Other means of identification

Product number -
Other names dibenzofuran-3,7-diamine

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:5896-30-0 SDS

5896-30-0Downstream Products

5896-30-0Relevant academic research and scientific papers

Effects of additional linkers in biphenyl-4,4′-dinitrene on the low-lying singlet-triplet energy gap and zero-field splitting

Nimura,Kikuchi,Ohana,Yabe,Kondo,Kaise

, p. 2083 - 2088 (2007/10/03)

Perturbation effects of additional linkers on the spin-spin coupling in biphenyl-4,4′-dinitrene (1) were examined by introducing a linking group between 2- and 2′-positions of 1. Five different doubly linked systems showed triplet ESR spectra corresponding to quinonoid dinitrenes. Curie law analyses suggested that all those triplet states were thermally excited triplet states. In addition, the singlet-triplet energy gaps, which were determined by the Curie law analyses, were well correlated with their corresponding zero-field-splitting (zfs) D values. The result could be explained by the stability of dinitrene character which is estimated from the resonance energy of the intervening π-system. Our semiempirical molecular orbital calculations supported the experimental correlation between the singlet-triplet energy gap and the zfs D value.

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