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71383-01-2

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71383-01-2 Usage

General Description

2,3-bis(dibromomethyl)naphthalene, also known as DBN, is a chemical compound used primarily as a flame retardant. It is a white to off-white solid with a distinct odor and is insoluble in water. DBN is utilized in a variety of industrial applications, including in the production of plastics, textiles, and foam products, to reduce the risk of fire and improve the fire resistance of these materials. It is considered to be a highly effective flame retardant due to its ability to release bromine radicals when exposed to heat, which can inhibit combustion and reduce the spread of flames. However, concerns have been raised about its potential environmental and health impacts, as brominated flame retardants like DBN are known to be persistent, bioaccumulative, and potentially toxic.

Check Digit Verification of cas no

The CAS Registry Mumber 71383-01-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,3,8 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71383-01:
(7*7)+(6*1)+(5*3)+(4*8)+(3*3)+(2*0)+(1*1)=112
112 % 10 = 2
So 71383-01-2 is a valid CAS Registry Number.

71383-01-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-bis(dibromomethyl)naphthalene

1.2 Other means of identification

Product number -
Other names 2,3-bis-dibromomethyl-naphthalene

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:71383-01-2 SDS

71383-01-2Relevant articles and documents

Intramolecular Singlet Fission in Oligoacene Heterodimers

Sanders, Samuel N.,Kumarasamy, Elango,Pun, Andrew B.,Steigerwald, Michael L.,Sfeir, Matthew Y.,Campos, Luis M.

, p. 3373 - 3377 (2016)

We investigate singlet fission (SF) in heterodimers comprising a pentacene unit covalently bonded to another acene as we systematically vary the singlet and triplet pair energies. We find that these energies control the SF process, where dimers undergo SF provided that the resulting triplet pair energy is similar or lower in energy than the singlet state. In these systems the singlet energy is determined by the lower-energy chromophore, and the rate of SF is found to be relatively independent of the driving force. However, triplet pair recombination in these heterodimers follows the energy gap law. The ability to tune the energies of these materials provides a key strategy to study and design new SF materials - an important process for third-generation photovoltaics. Organic electronics: A series of oligoacene heterodimers was synthesized to test the energetic requirements for singlet fission - a photophysical process that yields two triplet excitons from a single photon. Thus a possibility is offered to tune this process.

Synthesis of Benzo-Fused Tetraphenylenes and Crystal Structure of a 4:1 Clathrate Inclusion Compound of Dibenzotetraphenylene with p-Xylene

Man, Yuet-Ming,Mak, Thomas C. W.,Wong, Henry N. C.

, p. 3214 - 3221 (2007/10/02)

Benzo-fused tetraphenylenes 2-6 were successfully prepared by the combined deployment of the Diels-Alder cycloaddition between some strained cyclooctynes and furans and subsequent low-valent-titanium deoxygenation of the resulting 1,4-endoxides.As expecte

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