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519294

Sigma-Aldrich

1-Ethynyl-4-nitrobenzene

97%

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About This Item

Linear Formula:
HC≡CC6H4NO2
CAS Number:
937-31-5
Molecular Weight:
147.13
MDL number:
MFCD00024794
UNSPSC Code:
12352100
PubChem Substance ID:
24874071
NACRES:
NA.22

Quality Level

100

Assay

97%

mp

148-150 °C (lit.)

SMILES string

[O-][N+](=O)c1ccc(cc1)C#C

InChI

1S/C8H5NO2/c1-2-7-3-5-8(6-4-7)9(10)11/h1,3-6H

InChI key

GAZZTEJDUGESGQ-UHFFFAOYSA-N

Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Dipolar cross-linkers for PDMS networks with enhanced dielectric permittivity and low dielectric loss.
Madsen FB, et al.
Smart Materials and Structures, 22(10), 104002-104002 (2013)
Novel cross-linkers for PDMS networks for controlled and well distributed grafting of functionalities by click chemistry.
Madsen FB, et al.
Polym. Chem., 4(5), 1700-1707 (2013)
Synthesis of telechelic vinyl/allyl functional siloxane copolymers with structural control.
Madsen FB, et al.
Polym. Chem., 5(24), 7054-7061 (2014)
Fabiola Zapata et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(27), 9797-9808 (2015-06-03)
Several bis(triazolium)-based receptors have been synthesized as chemosensors for anion recognition. The central naphthalene core features two aryltriazolium side-arms. NMR experiments revealed differences between the binding modes of the two triazolium rings: one triazolium ring acts as a hydrogen-bond donor
Mohammad Zafar et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(59), 13537-13546 (2019-07-25)
Building upon previous work, the chemistry of [(η6 -p-cymene)Ru{P(OMe)2 OR}Cl2 ], (R=H or Me) has been extended with [H2 B(mbz)2 ]- (mbz=2-mercaptobenzothiazolyl) using different Ru precursors and borate ligands. As a result, a series of 1,3-N,S-chelated ruthenium borate complexes, for

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