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243264

Supelco

Nitron

98%

Synonym(s):

1,4-Diphenyl-3-phenylamino-1,2,4-triazolium hydroxide inner salt, 3,5,6-Triphenyl-2,3,5,6-tetraazabicyclo[2.1.1]hex-1-ene, 4,5-Dihydro-2,4-diphenyl-5-(phenylimino)-1H-1,2,4-triazolium hydroxide inner salt

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About This Item

Empirical Formula (Hill Notation):
C20H16N4
CAS Number:
2218-94-2
Molecular Weight:
312.37
Beilstein/REAXYS Number:
3913543
EC Number:
218-724-2
MDL number:
MFCD00005174
UNSPSC Code:
12352200
PubChem Substance ID:
329752630

assay

98%

mp

189-190 °C (dec.) (lit.)

SMILES string

[N-]1N(C=[N+](c2ccccc2)\C1=N\c3ccccc3)c4ccccc4

InChI

1S/C20H16N4/c1-4-10-17(11-5-1)21-20-22-24(19-14-8-3-9-15-19)16-23(20)18-12-6-2-7-13-18/h1-16H

Inchi Key

CWGBFIRHYJNILV-UHFFFAOYSA-N

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Product No.
Description
Pricing

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
S38277
S35750
12914TD
S28811
11114TC

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Attila Szebeni et al.
The international journal of neuropsychopharmacology, 17(10), 1579-1589 (2014-06-27)
Telomere shortening is observed in peripheral mononuclear cells from patients with major depressive disorder (MDD). Whether this finding and its biological causes impact the health of the brain in MDD is unknown. Brain cells have differing vulnerabilities to biological mechanisms
Einav Amit et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(57), 13046-13052 (2020-04-29)
N-heterocyclic carbenes (NHCs) have emerged as a unique molecular platform for the formation of self-assembled monolayers (SAMs) on various surfaces. However, active carbene formation requires deprotonation of imidazolium salt precursors, which is mostly facilitated by exposure of the salt to
Fuminori Yoneyama et al.
Bioengineered, 6(4), 209-217 (2015-04-17)
Glycerol is an interesting feedstock for biomaterials such as biofuels and bioplastics because of its abundance as a by-product during biodiesel production. Here we demonstrate glycerol metabolism in the nitrogen-fixing species Azotobacter vinelandii through metabolomics and nitrogen-free bacterial production of

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