43116
N-(Diphenylmethyl)methylamine
≥98.0% (GC)
Synonym(s):
N-Methylbenzhydrylamine
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About This Item
Empirical Formula (Hill Notation):
C14H15N
CAS Number:
Molecular Weight:
197.28
Beilstein:
2096409
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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
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)
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
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
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
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