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43116

Sigma-Aldrich

N-(Diphenylmethyl)methylamin

≥98.0% (GC)

Synonym(e):

N-Methylbenzhydrylamin

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About This Item

Empirische Formel (Hill-System):
C14H15N
CAS-Nummer:
14683-47-7
Molekulargewicht:
197.28
Beilstein:
2096409
MDL-Nummer:
MFCD00467853
UNSPSC-Code:
12352100
PubChem Substanz-ID:
57650145
NACRES:
NA.22

Assay

≥98.0% (GC)

Form

solid

mp (Schmelzpunkt)

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

InChIKey

SHDMMLFAFLZUEV-UHFFFAOYSA-N

Allgemeine Beschreibung

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

Piktogramme

Corrosion
GHS05

Signalwort

Danger

H-Sätze

H314

Gefahreneinstufungen

Skin Corr. 1B

Lagerklassenschlüssel

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

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α-Conotoxin Vc1.1 inhibits the nicotinic acetylcholine receptor (nAChR) α9α10 subtype and has the potential to treat neuropathic chronic pain. To date, the crystal structure of Vc1.1-bound α9α10 nAChR remains unavailable; thus, understanding the structure-activity relationship of Vc1.1 with the α9α10
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Analytical biochemistry, 536, 59-68 (2017-08-15)
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PloS one, 13(4), e0195802-e0195802 (2018-04-19)
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An Improved Iron-Catalyzed Epoxidation of Aromatic and Aliphatic Olefins with Hydrogen Peroxide as Oxidant.
Bitterlich B, et al.
European Journal of Organic Chemistry, 29, 4867-4870 (2008)
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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
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