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Merck

17356

3-(Boc-amino)propyl bromide

≥96.0% (GC)

Synonym(s):

tert-Butyl N-(3-bromopropyl)carbamate

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About This Item

Linear Formula:
Br(CH2)3NHCO2C(CH3)3
CAS Number:
Molecular Weight:
238.12
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4176344
Assay:
≥96.0% (GC)
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Quality Segment

assay

≥96.0% (GC)

reaction suitability

reagent type: cross-linking reagent

mp

37-39 °C

functional group

Boc, amine, bromo

storage temp.

2-8°C

SMILES string

BrCCCNC(OC(C)(C)C)=O

InChI

1S/C8H16BrNO2/c1-8(2,3)12-7(11)10-6-4-5-9/h4-6H2,1-3H3,(H,10,11)

InChI key

IOKGWQZQCNXXLD-UHFFFAOYSA-N

Application

3-(Boc-amino)propyl bromide can be used as an alkylating reagent for the synthesis of:
  • Benzydamine analogs to be used as activators for soluble guanylate cyclase.
  • N-substituted chromenotriazolopyrimidine, human murine double minute 2 (MDM2) inhibitor.
  • Protected amines from piperidine derivatives to be further used for synthesis of sulfonamide series.

It can also be used for the post-polymerization quaternization of polymers to synthesize functional cationic polymers and antimicrobial agents.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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