17356

3-(Boc-amino)propyl bromide

≥96.0% (GC)

• Synonym(s): tert-Butyl N-(3-bromopropyl)carbamate
• Linear Formula: Br(CH₂)₃NHCO₂C(CH₃)₃
• CAS Number: 83948-53-2
• Molecular Weight: 238.12
• Beilstein/REAXYS Number: 4176344
• MDL number: MFCD02683429
• PubChem Substance ID: 57647642
• NACRES: NA.22

Properties

• Quality Level: 200
• assay: ≥96.0% (GC)
• reaction suitability: reagent type: cross-linking reagent; reagent type: spacer
• mp: 37-39 °C
• storage temp.: 2-8°C
• SMILES string: CC(C)(C)OC(=O)NCCCBr
• 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

Description

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.

Packaging

2.5 g in poly bottle

500 mg in poly bottle

Safety Information

• Pictograms: GHS07
• Signal Word: Warning
• Hazard Statements: H302 - H315 - H319 - H335
• Precautionary Statements: P301 + P312 + P330 - P302 + P352 - P305 + P351 + P338
• Target Organs: Respiratory system
• Personal Protective Equipment: dust mask type N95 (US),Eyeshields,Gloves
• RIDADR: NONH for all modes of transport
• WGK Germany: WGK 3
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable