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Diazene, bis[4-(bromomethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 97654-99-4 Structure
  • Basic information

    1. Product Name: Diazene, bis[4-(bromomethyl)phenyl]-
    2. Synonyms: 4,4'-bis(bromomethyl)azobenzene;trans-1,1'-azobis(4-bromomethylbenzene);(E)-4,4'-bis(bromomethyl)azobenzene;Diazene,bis[4-(bromomethyl)phenyl];bis(4-bromomethylphenyl)diazene;
    3. CAS NO:97654-99-4
    4. Molecular Formula: C14H12Br2N2
    5. Molecular Weight: 368.071
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 97654-99-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Diazene, bis[4-(bromomethyl)phenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Diazene, bis[4-(bromomethyl)phenyl]-(97654-99-4)
    11. EPA Substance Registry System: Diazene, bis[4-(bromomethyl)phenyl]-(97654-99-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 97654-99-4(Hazardous Substances Data)

97654-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97654-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,6,5 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 97654-99:
(7*9)+(6*7)+(5*6)+(4*5)+(3*4)+(2*9)+(1*9)=194
194 % 10 = 4
So 97654-99-4 is a valid CAS Registry Number.

97654-99-4SDS

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 bis[4-(bromomethyl)phenyl]diazene

1.2 Other means of identification

Product number -
Other names (E)-4,4'-bis(bromomethyl)azobenzene

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:97654-99-4 SDS

97654-99-4Relevant articles and documents

A novel azobenzene-based fluorescent sensor for selective detection of mercury ion

Gao, Yan,Song, Jian,Wang, Wei

, p. 749 - 751 (2011)

A highly sensitive fluorescent probe (3) for selective detection of mercury based on an azobenzene derivative with 1,3,4-triazole units has been designed, synthesized, and examined for their cation recognition abilities toward various cations by UV-vis, f

Photoswitchable Conjugated Oligoelectrolytes for a Light-Induced Change of Membrane Morphology

Bazan, Guillermo C.,Leifert, Dirk,Limwongyut, Jakkarin,Mikhailovsky, Alexander A.,Moreland, Alex S.

, p. 20333 - 20337 (2020/09/07)

The synthesis of a new conjugated oligoelectrolyte (COE), namely DSAzB, is described, which contains a conjugated core bearing a diazene moiety in the center of its electronically delocalized structure. Similar to structurally related phenylenevinylene-based COEs, DSAzB readily intercalates into model and natural lipid bilayer membranes. Photoinduced isomerization transforms the linear trans COE into a bent or C-shape form. It is thereby possible to introduce DSAzB into the bilayer of a cell and disrupt its integrity by irradiation with light. This leads to controlled permeabilization of membranes, as demonstrated by the release of calcein from DMPG/DMPC vesicles and by propidium iodide influx experiments on S. epidermidis. Both experiments support that the permeabilization is selective for the light stimulus, highly efficient, and repeatable. Target-selective and photoinduced actions demonstrated by DSAzB may have broad applications in biocatalysis and related biotechnologies.

Optical Control of Cardiac Function with a Photoswitchable Muscarinic Agonist

Riefolo, Fabio,Matera, Carlo,Garrido-Charles, Aida,Gomila, Alexandre M. J.,Sortino, Rosalba,Agnetta, Luca,Claro, Enrique,Masgrau, Roser,Holzgrabe, Ulrike,Batlle, Montserrat,Decker, Michael,Guasch, Eduard,Gorostiza, Pau

, p. 7628 - 7636 (2019/05/16)

Light-triggered reversible modulation of physiological functions offers the promise of enabling on-demand spatiotemporally controlled therapeutic interventions. Optogenetics has been successfully implemented in the heart, but significant barriers to its u

Azobenzene-Bridged Expanded "Texas-sized" Box: A Dual-Responsive Receptor for Aryl Dianion Encapsulation

Chi, Xiaodong,Cen, Wanglai,Queenan, Jack A.,Long, Lingliang,Lynch, Vincent M.,Khashab, Niveen M.,Sessler, Jonathan L.

, p. 6468 - 6472 (2019/05/06)

We report an expanded "Texas-sized" molecular box (AzoTxSB) that incorporates photoresponsive azobenzene bridging subunits and anion recognition motifs. The shape of this box can be switched through light induced E ? Z photoisomerization of the constituen

Dimeric surfactant containing azobenzene group, and application thereof

-

, (2019/07/04)

The invention discloses a dimeric surfactant containing an azobenzene group, and an application thereof, and belongs to the fields of surfactant science and application technologies thereof. Sodium oleate and a dimeric quaternary ammonium salt are compoun

Fluorination of Photoswitchable Muscarinic Agonists Tunes Receptor Pharmacology and Photochromic Properties

Agnetta, Luca,Bermudez, Marcel,Riefolo, Fabio,Matera, Carlo,Claro, Enrique,Messerer, Regina,Littmann, Timo,Wolber, Gerhard,Holzgrabe, Ulrike,Decker, Michael

, p. 3009 - 3020 (2019/05/08)

Red-shifted azobenzene scaffolds have emerged as useful molecular photoswitches to expand potential applications of photopharmacological tool compounds. As one of them, tetra-ortho-fluoro azobenzene is well compatible for the design of visible-light-responsive systems, providing stable and bidirectional photoconversions and tissue-compatible characteristics. Using the unsubstituted azobenzene core and its tetra-ortho-fluorinated analogue, we have developed a set of uni- and bivalent photoswitchable toolbox derivatives of the highly potent muscarinic acetylcholine receptor agonist iperoxo. We investigated the impact of the substitution pattern on receptor activity and evaluated the different binding modes. Compounds 9b and 15b show excellent photochemical properties and biological activity as fluorination of the azobenzene core alters not only the photochromic behavior but also the pharmacological profile at the muscarinic M1 receptor. These findings demonstrate that incorporation of fluorinated azobenzenes not just may alter photophysical properties but can exhibit a considerably different biological profile that has to be carefully investigated.

Comparison of computationally cheap methods for providing insight into the crystal packing of highly bromomethylated azobenzenes

Vande Velde, Christophe M. L.,Zeller, Matthias,Azov, Vladimir A.

, p. 1692 - 1702 (2018/11/30)

For five bromomethylated azobenzenes, namely (E)-[4-(bromomethyl)phenyl][4-(dibromomethyl)phenyl]diazene, C14H11Br3N2, (E)-1,2-bis[4-(dibromomethyl)phenyl]diazene, C14H10Br4Nsub

A photo-responsive poly(amide-triazole) physical organogel bearing azobenzene residues in the main chain

Wang, Huai-Zhen,Chow, Hak-Fun

, p. 8391 - 8394 (2018/08/01)

The synthesis of a click poly(amide-triazole) bearing multiple azobenzene units along the main chain was reported. The polymer was found to form strong physical polymer organogels. This structural design facilitates a much more efficient photomechanical e

Insights into the Difference Between Rotaxane and Pseudorotaxane

Sun, He-Lue,Zhang, Heng-Yi,Dai, Zhen,Han, Xu,Liu, Yu

supporting information, p. 265 - 270 (2017/02/05)

Rotaxane and pseudorotaxane are two types of mechanically interlocked molecular architectures, and there is a clear topological difference and boundary between them. In this work, a “suggested [2]rotaxane 1?α-CD” was constructed based on axle molecule 1 b

Switching Process Consisting of Three Isomeric States of an Azobenzene Unit

Adam, Abdulselam,Haberhauer, Gebhard

, p. 9708 - 9713 (2017/07/24)

Azobenzene and its derivatives are among the most commonly used switching units in organic chemistry. The switching process consists of two states, in which the trans isomer has a stretched and the cis isomer a compact form. Here, we have designed a syste

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