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325430

Sigma-Aldrich

Triphenylmethylamine

99%

Sinónimos:

Tritylamine

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About This Item

Fórmula lineal:
(C6H5)3CNH2
Número de CAS:
5824-40-8
Peso molecular:
259.34
Beilstein/REAXYS Number:
2113674
MDL number:
MFCD00008047
UNSPSC Code:
12352100
PubChem Substance ID:
24859510
NACRES:
NA.22

assay

99%

form

solid

bp

223 °C/14 mmHg (lit.)

mp

102-104 °C (lit.)

SMILES string

NC(c1ccccc1)(c2ccccc2)c3ccccc3

InChI

1S/C19H17N/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H,20H2

InChI key

BZVJOYBTLHNRDW-UHFFFAOYSA-N

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Categorías relacionadas

General description

Reaction of triphenylmethylamine with borontrifluoride was studied.

Application

Triphenylmethylamine was used to prepare diamondoid porous organic salt. It was also used in preparation of N-tritylated β-aminoalcohols, useful building blocks in organic synthesis.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Tritylamine (triphenylmethylamine) in organic synthesis; II. The reaction of tritylamine with oxiranes-synthesis of N-trityl-? aminoalcohols.
Soroka M and Goldeman W.
ARKIVOC (Gainesville, FL, United States), 12, 31-37 (2003)
Reaction of triphenylmethylamines with boron trihalides.
Ronan RJ, et al.
Journal of the American Chemical Society, 93(25), 6811-6814 (1971)
Atsushi Yamamoto et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(9), 3006-3016 (2013-01-12)
A diamondoid porous organic salt (d-POS) composed of 8-hydroxyquinoline-5-sulfonic acid (HQS) and triphenylmethylamine (TPMA) shows reversible structure contraction and expansion ("breathing") in response to guest desorption and adsorption. This flexible structure is designed hierarchically by utilizing two different types of
Grant A McNaughton-Smith et al.
Journal of medicinal chemistry, 51(4), 976-982 (2008-02-01)
Sickle cell disease (SCD) is a hereditary condition characterized by deformation of red blood cells (RBCs). This phenomenon is due to the presence of abnormal hemoglobin that polymerizes upon deoxygenation. This effect is exacerbated when dehydrated RBCs experience a loss
Silke B Bodendiek et al.
Frontiers in pharmacology, 3, 106-106 (2012-06-12)
The paucity of specific pharmacological agents has been a major impediment for delineating the roles of gap junction (GJ) channels formed by connexin proteins in physiology and pathophysiology. Here, we used the selective optimization of side activities (SOSA) approach, which
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