17356
3-(Boc-amino)propyl bromide
≥96.0% (GC)
Synonym(s):
tert-Butyl N-(3-bromopropyl)carbamate
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About This Item
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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
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This Item | 17354 | 89171 | 15408 |
|---|---|---|---|
| assay ≥96.0% (GC) | assay ≥97.0% (GC) | assay ≥97.0% (GC) | assay ≥97.0% (GC/NT) |
| Quality Level 200 | Quality Level 200 | Quality Level 100 | Quality Level 100 |
| reaction suitability reagent type: cross-linking reagent | reaction suitability reagent type: cross-linking reagent | reaction suitability reagent type: cross-linking reagent | reaction suitability reagent type: cross-linking reagent |
| mp 37-39 °C | mp 30-32 °C (lit.) | mp - | mp 22 °C (lit.) |
| storage temp. 2-8°C | storage temp. −20°C | storage temp. - | storage temp. - |
| functional group Boc | functional group Boc, amine, bromo | functional group Boc, amine, bromo | functional group Boc, amine |
Application
- Benzydamine analogs to be used as activators for soluble guanylate cyclase.[1]
- N-substituted chromenotriazolopyrimidine, human murine double minute 2 (MDM2) inhibitor.[2]
- Protected amines from piperidine derivatives to be further used for synthesis of sulfonamide series.[3]
It can also be used for the post-polymerization quaternization of polymers to synthesize functional cationic polymers and antimicrobial agents.[4]
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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