B9602
二苯甲酮腙
96%
别名:
二苯基重氮甲烷前体
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关于此项目
线性分子式:
(C6H5)2C=NNH2
化学文摘社编号:
分子量:
196.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-321-8
Beilstein/REAXYS Number:
1910177
MDL number:
产品名称
二苯甲酮腙, 96%
InChI key
QYCSNMDOZNUZIT-UHFFFAOYSA-N
InChI
1S/C13H12N2/c14-15-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H,14H2
SMILES string
N\N=C(/c1ccccc1)c2ccccc2
assay
96%
form
crystals
bp
225-230 °C/55 mmHg (lit.)
mp
95-98 °C (lit.)
storage temp.
2-8°C
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
294.8 °F
flash_point_c
146 °C
ppe
Eyeshields, Gloves, type N95 (US)
Synthesis and urease inhibitory potential of benzophenone sulfonamide hybrid in vitro and in silico.
Arshia et al.
Bioorganic & medicinal chemistry, 27(6), 1009-1022 (2019-02-11)
This study deals with the synthesis of benzophenone sulfonamides hybrids (1-31) and screening against urease enzyme in vitro. Studies showed that several synthetic compounds were found to have good urease enzyme inhibitory activity. Compounds 1 (N'-((4'-hydroxyphenyl)(phenyl)methylene)-4''-nitrobenzenesulfonohydrazide), 2 (N'-((4'-hydroxyphenyl)(phenyl)methylene)-3''-nitrobenzenesulfonohydrazide), 3 (N'-((4'-hydroxyphenyl)(phenyl)methylene)-4''-methoxybenzenesulfonohydrazide)
Fatemeh M Mir et al.
Journal of medicinal chemistry, 62(9), 4500-4525 (2019-04-02)
Peptide mimicry employing a combination of aza-amino acyl proline and indolizidinone residues has been used to develop allosteric modulators of the prostaglandin F2α receptor. The systematic study of the N-terminal phenylacetyl moiety and the conformation and side chain functions of
Kelvine Chignen Possi et al.
Journal of medicinal chemistry, 60(22), 9263-9274 (2017-10-14)
Azapeptide analogues of growth hormone releasing peptide-6 (GHRP-6) exhibit promising affinity, selectivity, and modulator activity on the cluster of differentiation 36 receptor (CD36). For example, [A
Ngoc-Duc Doan et al.
Journal of peptide science : an official publication of the European Peptide Society, 21(5), 387-391 (2014-11-18)
The solid-phase synthesis of azapeptides possessing a C-terminal aza-residue has been accomplished by a protocol featuring regioselective alkylation of benzhydrylidene-aza-glycinamide and illustrated by the syntheses of [aza-Lys(6)] growth-hormone-releasing peptide-6 analogs.
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