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102437-80-9

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102437-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102437-80-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,3 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 102437-80:
(8*1)+(7*0)+(6*2)+(5*4)+(4*3)+(3*7)+(2*8)+(1*0)=89
89 % 10 = 9
So 102437-80-9 is a valid CAS Registry Number.

102437-80-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-bis(azidomethyl)benzene

1.2 Other means of identification

Product number -
Other names m-xylylene diazide

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:102437-80-9 SDS

102437-80-9Relevant academic research and scientific papers

Preparation of thermocleavable conjugates based on ansamitocin and superparamagnetic nanostructured particles by a chemobiosynthetic approach

Mancuso, Lena,Knobloch, Tobias,Buchholz, Jessica,Hartwig, Jan,M?ller, Lena,Seidel, Katja,Collisi, Wera,Sasse, Florenz,Kirschning, Andreas

, p. 17541 - 17551 (2014)

A combination of mutasynthesis, precursor-directed biosynthesis and semisynthesis provides access to new ansamitocin derivatives including new nanostructured particle-drug conjugates. These conjugates are based on the toxin ansamitocin and superparamagnetic iron oxide-silica core shell particles. New ansamitocin derivatives that are functionalized either with alkynylor azido groups in the ester side chain at C-3 are attached to nanostructured iron oxide core-silica shell particles. Upon exposure to an oscillating electromagnetic field these conjugates heat up and the ansamitocin derivatives are released by a retro-Diels-Alder reaction. For example, one ansamitocin derivative exerts strong antiproliferative activity against various cancer cell lines in the lower nanomolar range while the corresponding nanostructured particle-drug conjugate is not toxic. Therefore, these new conjugates can serve as dormant toxins that can be employed simultaneously in hyperthermia and chemotherapy when external inductive heating is applied.

Design, synthesis and application of new bile acid ligands with 1,2,3-triazole ring

Pospieszny, Tomasz,Pakiet, Marta,Kowalczyk, Iwona,Brycki, Bogumi?

, p. 81 - 93 (2017)

New dimers have been obtained from propargyl ester of bile acids and α,α′-diazide-m-xylene by intermolecular 1,3-dipolar cycloaddition. These compounds have been used as ligands to form intermolecular hydrogen bonds with various aromatic acids. The struct

Design, synthesis, and self-assembling properties of novel triazolophanes

Haridas,Lal, Kashmiri,Sharma, Yogesh K.,Upreti, Shailesh

, p. 1645 - 1647 (2008)

A series of novel triazolophanes containing peptidic and nonpeptidic backbones is reported. The crystal structure of one such macrocycle displays self-assembly through nonconventional hydrogen-bonding interactions.

Design, synthesis, antimicrobial evaluation and in silico studies of symmetrical bis (urea-1,2,3-triazole) hybrids

Poonia, Nisha,Lal, Kashmiri,Kumar, Ashwani

, p. 1087 - 1103 (2021)

Abstract: In search of 1,2,3-triazole-based antimicrobials, some symmetrical bis(urea-1,2,3-triazole) hybrids were synthesized via clicked Huisgen cycloaddition. The structural characterization was done by different physical and spectral techniques like N

Phosphatidylcholine-derived bolaamphiphiles via click chemistry

O'Neil, Edward J.,DiVittorio, Kristy M.,Smith, Bradley D.

, p. 199 - 202 (2007)

(Chemical Equation Presented) The copper-catalyzed azide alkyne cycloaddition is employed to modify phosphatidylcholine precursors with sn-2 acyl chains containing terminal alkyne or azide groups. Although the reactions are conducted as biphasic dispersio

Bicyclic Picomolar OGA Inhibitors Enable Chemoproteomic Mapping of Its Endogenous Post-translational Modifications

Ashmus, Roger A.,Busmann, Jil A.,Davies, Gideon J.,Foster, Leonard J.,García Fernández, José M.,González-Cuesta, Manuel,Madden, Zarina,Males, Alexandra,Ortiz Mellet, Carmen,Proceviat, Cameron,Rogalski, Jason C.,Sidhu, Peter,Vocadlo, David J.

supporting information, p. 832 - 844 (2022/01/19)

Owing to its roles in human health and disease, the modification of nuclear, cytoplasmic, and mitochondrial proteins with O-linked N-acetylglucosamine residues (O-GlcNAc) has emerged as a topic of great interest. Despite the presence of O-GlcNAc on hundre

Charge neutral halogen bonding tetradentate-iodotriazole macrocycles capable of anion recognition and sensing in highly competitive aqueous media

Beer, Paul D.,Boonpalit, Kajjana,Bunchuay, Thanthapatra,Docker, Andrew,Ruengsuk, Araya,Sukwattanasinitt, Mongkol,Surawatanawong, Panida,Tantirungrotechai, Jonggol

supporting information, p. 11976 - 11979 (2021/12/01)

A series of neutral tetradentate halogen bonding (XB) macrocycles, comprising of two bis-iodotriazole XB donors were synthesised in 60-70% yields via a stepwise CuAAC-mediated cyclisation strategy. Extensive 1H NMR anion titration experiments reveal halide binding affinities are critically dependent on the substitution pattern of the xylyl spacer unit. The meta-substituted macrocycle remarkably displays cooperative tetradentate XB-halide anion recognition in highly competitive 40% aqueous-organic D2O/acetone-d6 (40?:?60, v/v) solvent mixtures. Integration of para-xylyl and naphthyl spacer units generates extended macrocyclic cavities, capable of selective oxalate recognition. Furthermore, preliminary fluorescence exeperiments reveal dicarboxylate specific sensing can be achieved through monitoring of the naphthylene centred emission. This journal is

Synthesis, anti-microbial activity and molecular docking studies on triazolylcoumarin derivatives

Satheeshkumar, Chinnadurai,Ravivarma, Mahalingam,Arjun, Pandian,Silambarasan, Vaithiyanathan,Raaman, Nanjian,Velmurugan, Devadasan,Song, Changsik,Rajakumar, Perumal

, p. 565 - 571 (2015/05/20)

A series of triazolylcoumarins was synthesized by the cycloaddition of acetylenic derivatives to azide in the presence of Cu(I) catalyst at room temperature. All the synthesized compounds were evaluated for their anti-microbial activity against Gram-posit

Detection of Zn(II) ions by fluorescent pyrene-derived molecular probes

Manandhar, Erendra,Cragg, Peter J.,Wallace, Karl J.

, p. 141 - 150 (2014/05/06)

Two pyrene-based molecular probes have been synthesised from ortho-and meta-bis(azidodimethyl)benzene and their coordination with Fe(III), Al(III), Fe(II), Zn(II), Ni(II), Cu(II), Cd(II), Hg(II), Ca(II), Mg(II) and Na(I) cations is described. The greatest

Bi- and tri-metallic Rh and Ir complexes containing click derived bis- and tris-(pyrazolyl-1,2,3-triazolyl) N-N′ donor ligands and their application as catalysts for the dihydroalkoxylation of alkynes

Vuong, Khuong Q.,Wong, Chin M.,Bhadbhade, Mohan,Messerle, Barbara A.

supporting information, p. 7540 - 7553 (2014/05/20)

A series of bi-topic and tri-topic pyrazolyl-1,2,3-triazolyl donor ligands (1a-d; 1a-c = 1,X-bis((4-((1H-pyrazol-1-yl)methyl)-1H-1,2,3-triazol-1-yl)methyl) benzene (X = 2, 3 and 4; o-C6H4(PyT)2, m-C 6H4/su

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