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Merck
CN

43116

N-(二苯甲基)甲胺

≥98.0% (GC)

别名:

N-甲基二甲苯胺

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关于此项目

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
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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.

pictograms

Corrosion

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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)
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

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