P27100
N-フェニルマレイミド
97%
別名:
1-Phenyl-pyrrole-2,5-dione, 1-[4-(Acetoxy)phenyl]maleimide
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この商品について
実験式（ヒル表記法）:
C10H7NO2
CAS番号:
分子量:
173.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-382-0
Beilstein/REAXYS Number:
125098
MDL number:
Assay:
97%
Form:
solid
Quality Level
assay
97%
form
solid
bp
162-163 °C/12 mmHg (lit.)
mp
85-87 °C (lit.)
SMILES string
O=C1C=CC(=O)N1c2ccccc2
InChI
1S/C10H7NO2/c12-9-6-7-10(13)11(9)8-4-2-1-3-5-8/h1-7H
InChI key
HIDBROSJWZYGSZ-UHFFFAOYSA-N
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Acute 1
保管分類
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
第一種指定化学物質
prtr
名称等を表示すべき危険物及び有害物
ishl_indicated
名称等を通知すべき危険物及び有害物
ishl_notified
P27100-25G: + P27100-VAR: + P27100-100G: + P27100-1KG: + P27100-BULK:
jan
Jian-Hui Wen et al.
Talanta, 84(1), 13-18 (2011-02-15)
Representing a compound by a numerous structural descriptors becomes common in quantitative structure-activity relationship (QSAR) studies. As every descriptor carries molecular structure information more or less, it seems more advisable to investigate all the possible descriptor vectors rather than traditional
Vânia F Noldin et al.
Pharmacological reports : PR, 63(3), 772-780 (2011-08-23)
Myeloperoxidase (MPO) is an important enzyme that catalyzes the reaction between hydrogen peroxide and chloride to generate hypochlorous acid, which oxidizes a range of biomolecules and has been associated with inflammatory diseases. The synthetic compounds N-phenylmaleimide (NFM) and 4-methyl-N-phenylmaleimide (Me-NFM)
Yan Wang et al.
The Journal of organic chemistry, 77(8), 4143-4147 (2012-04-05)
A Me-DuPhos-catalyzed efficient asymmetric [3 + 2] cycloaddition reaction between Morita-Baylis-Hillman carbonates of isatins and N-phenylmaleimide has been developed. This reaction constructs three chiral centers in one step to afford spirocyclopentaneoxindoles in good yields (up to 84%) with excellent diastereo-