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T83607

Sigma-Aldrich

Bromotriphenylmethane

98%

Synonym(s):

Triphenylbromomethane, Trityl bromide

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About This Item

Linear Formula:
(C6H5)3CBr
CAS Number:
596-43-0
Molecular Weight:
323.23
Beilstein/REAXYS Number:
1878494
EC Number:
209-884-4
MDL number:
MFCD00000120
UNSPSC Code:
12352100
PubChem Substance ID:
24900521
NACRES:
NA.22

Quality Level

100

assay

98%

bp

230 °C/15 mmHg (lit.)

mp

152-154 °C (lit.)

storage temp.

2-8°C

SMILES string

BrC(c1ccccc1)(c2ccccc2)c3ccccc3

InChI

1S/C19H15Br/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

InChI key

NZHXEWZGTQSYJM-UHFFFAOYSA-N

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Related Categories

Application

Reagent for the preparation of trityl esters.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
STBK5831
STBK2891
STBK2272
STBH3141
STBG7881

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Siddabasave Gowda B Gowda et al.
Lipids, 55(4), 395-401 (2020-05-15)
An efficient three-step strategy for the convenient synthesis of Sn-glycero-3-phosphoethanolamine (GroPEtn) from a commercially available 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine (DPPE) is reported. Direct hydrolysis of DPPE produces a complex inseparable mixture, hence a protection and deprotection strategy is employed to prepare GroPEtn. The
Krzysztof Matyjaszewski et al.
Molecules (Basel, Switzerland), 26(2) (2021-01-14)
N-alkyl phosphoranimines were synthesized via the Staudinger reaction of four different alkyl azides with tris(2,2,2-trifluoroethyl) phosphite. N-adamantyl, N-benzyl, N-t-butyl, and N-trityl phosphoranimines were thoroughly characterized and evaluated as chain-capping compounds in the anionic polymerization of P-tris(2,2,2-trifluoroethoxy)-N-trimethylsilyl phosphoranimine monomer. All four
Yusuke Yamamoto et al.
Analytical and bioanalytical chemistry, 413(1), 245-254 (2020-10-23)
Lysophosphatidylethanolamines (LysoPEs) are the partial hydrolysis products of phosphatidylethanolamine. Despite the unique in vitro bioactivities of LysoPEs, there are limited reports on the pathophysiological role of LysoPEs in the serum, due to the lack of sensitive analytical methods for determination
Cansu Aydogan et al.
Macromolecular rapid communications, 40(14), e1900109-e1900109 (2019-05-16)
A straightforward transformation protocol combining two distinct living polymerization methods for the controlled synthesis of block copolymers is described. In the first step, bromo-terminated poly(methyl methacrylate) is prepared by atom transfer radical polymerization (ATRP). Then, a bromide end group is
Salvatore Debonis et al.
Journal of medicinal chemistry, 51(5), 1115-1125 (2008-02-13)
The human kinesin Eg5 is a potential drug target for cancer chemotherapy. Eg5 specific inhibitors cause cells to block in mitosis with a characteristic monoastral spindle phenotype. Prolonged metaphase block eventually leads to apoptotic cell death. S-trityl-L-cysteine (STLC) is a

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