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252611

N-(溴甲基)邻苯二甲酰亚胺

96%

别名:

N-溴甲基酞酰亚胺

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关于此项目

经验公式（希尔记法）:
C9H6BrNO2
化学文摘社编号:
5332-26-3
分子量:
240.05
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24855225
EC Number:
226-239-2
Beilstein/REAXYS Number:
140943
MDL number:
MFCD00005897
Assay:
96%
Form:
solid
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Quality Level

100

assay

96%

form

solid

mp

152-155 °C (lit.)

functional group

bromo, imide

SMILES string

BrCN1C(=O)c2ccccc2C1=O

InChI

1S/C9H6BrNO2/c10-5-11-8(12)6-3-1-2-4-7(6)9(11)13/h1-4H,5H2

InChI key

UUSLLECLCKTJQF-UHFFFAOYSA-N

Application

N-(Bromomethyl)phthalimide was used as initiator in synthesis of α-phthalimidopoly(styrene) by atom transfer radical polymerisation. It was also used in synthesis of functionalized 5-(aminomethyl)pyrimidine-2,4,6-trione analog and new bis-C(cage)-substituted o-carborane.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCX5990
MKCT5777
MKCJ1862
MKCC0906
MKCG1525

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Approaches to phthalimido and amino end-functional polystyrene by atom transfer radical polymerisation (ATRP).
Postma A, et al.
Reactive functional Polymers, 66(1), 137-147 (2006)
James J-W Duan et al.
Bioorganic & medicinal chemistry letters, 17(1), 266-271 (2006-10-10)
Using a pyrimidine-2,4,6-trione motif as a zinc-binding group, a series of selective inhibitors of tumor necrosis factor-alpha converting enzyme (TACE) was discovered. Optimization of initial lead 1 resulted in a potent inhibitor (51), with an IC(50) of 2 nM in
Synthesis and crystal structure of 1, 2-bis (phthalimidomethyl)-1, 2-dicarba-closo-dodecaborane (12): a precursor to polyamines.
Zhu Y, et al.
Inorganic Chemistry Communications, 4(8), 447-449 (2001)
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全球贸易项目编号

货号GTIN
252611-25G04061825973524
252611-5G04061825973531