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252611

Sigma-Aldrich

N-(Bromomethyl)phthalimide

96%

Synonym(s):

Phthalimidomethyl bromide

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About This Item

Empirical Formula (Hill Notation):
C9H6BrNO2
CAS Number:
5332-26-3
Molecular Weight:
240.05
Beilstein:
140943
EC Number:
226-239-2
MDL number:
MFCD00005897
UNSPSC Code:
12352100
PubChem Substance ID:
24855225
NACRES:
NA.22

Assay

96%

form

solid

mp

152-155 °C (lit.)

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

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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

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Polymeric biomaterials capable of delivering nitric oxide (NO) topically can be used to enhance skin blood flow (SkBF) and accelerate wound healing. Herein, we used reversible addition-fragmentation chain transfer radical (RAFT) polymerization to synthesize the first poly(vinyl alcohol) (PVA) functionalized
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