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经验公式(希尔记法):
C14H15N
化学文摘社编号:
分子量:
197.28
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2096409
Assay:
≥98.0% (GC)
Form:
solid
产品名称
N-(二苯甲基)甲胺, ≥98.0% (GC)
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
SMILES string
CNC(c1ccccc1)c2ccccc2
InChI key
SHDMMLFAFLZUEV-UHFFFAOYSA-N
assay
≥98.0% (GC)
form
solid
mp
38-42 °C
functional group
amine
phenyl
Quality Level
General description
N-(Diphenylmethyl)methylamine is a sterically hindered secondary amine. It participates in the synthesis of cyclooctene oxide.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
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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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
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)
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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
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