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Merck

43116

Sigma-Aldrich

N-(Diphenylmethyl)methylamine

≥98.0% (GC)

Sinónimos:

N-Methylbenzhydrylamine

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About This Item

Fórmula empírica (notación de Hill):
C14H15N
Número de CAS:
Peso molecular:
197.28
Beilstein/REAXYS Number:
2096409
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

≥98.0% (GC)

form

solid

mp

38-42 °C

SMILES string

CNC(c1ccccc1)c2ccccc2

InChI

1S/C14H15N/c1-15-14(12-8-4-2-5-9-12)13-10-6-3-7-11-13/h2-11,14-15H,1H3

InChI key

SHDMMLFAFLZUEV-UHFFFAOYSA-N

General description

N-(Diphenylmethyl)methylamine is a sterically hindered secondary amine. It participates in the synthesis of cyclooctene oxide.

pictograms

Corrosion

signalword

Danger

hcodes

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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Ganesan Rajasekaran et al.
Biochimica et biophysica acta, 1859(5), 722-733 (2017-02-06)
Although the human-derived antimicrobial peptide (AMP) LL-37 has potent antimicrobial and anti-inflammatory activities, its therapeutic application is limited by its low cell selectivity and high production cost due to its large size. To overcome these problems, we tried to develop
Eun Young Kim et al.
European journal of medicinal chemistry, 136, 428-441 (2017-05-20)
KR-12-a5 is a 12-meric α-helical antimicrobial peptide (AMP) with dual antimicrobial and anti-inflammatory activities designed from human cathelicidin LL-37. We designed and synthesized a series of d-amino acid-substituted analogs of KR-12-a5 with the aim of developing novel α-helical AMPs that
N-Diphenylmethyl-2-propenamide: theoretical study of the structure and interaction with a DNA model system.
Barone G, et al.
Journal of Molecular Structure, 572(1), 113-119 (2001)
He Ma et al.
ChemMedChem, 14(19), 1710-1716 (2019-08-25)
Naturally occurring constrained peptides are frequently used as scaffolds for bioactive peptide grating due to their high stability. Here, we used in silico methods to design several constrained peptides comprising a scorpion toxin scaffold, a MDM2 binding epitope, and a
Svetlana N Rylova et al.
PloS one, 13(4), e0195802-e0195802 (2018-04-19)
Copper-64 is an attractive radionuclide for PET imaging and is frequently used in clinical applications. The aim of this study was to perform a side-by-side comparison of the in vitro and in vivo performance of 64Cu-NODAGA-JR11 (NODAGA = 1,4,7-triazacyclononane,1-glutaric acid,4,7-acetic

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