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519294

1-Ethynyl-4-nitrobenzene

Name: 1-Ethynyl-4-nitrobenzene
Brand: ALDRICH

97%

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About This Item

Linear Formula:

HC≡CC₆H₄NO₂

CAS Number:

937-31-5

Molecular Weight:

147.13

NACRES:

NA.22

PubChem Substance ID:

24874071

UNSPSC Code:

12352100

MDL number:

MFCD00024794

Assay:

97%

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Properties

Quality Level

100

assay

97%

mp

148-150 °C (lit.)

functional group

nitro

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

Description

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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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)

Dual Role of the 1,2,3-Triazolium Ring as a Hydrogen-Bond Donor and Anion-π Receptor in Anion-Recognition Processes.

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

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Global Trade Item Number

SKU	GTIN
519294-5G	04061832544359
519294-1G	04061832544335