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90303

Sigma-Aldrich

4-(Boc-amino)butyl bromide

technical, ≥90% (AT)

Synonym(s):

Carbamic acid, (4-bromobutyl)-, 1,1-dimethylethyl ester, tert-Butyl N-(4-bromobutyl)carbamate

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About This Item

Linear Formula:
Br(CH2)4NHCO2C(CH3)3
CAS Number:
164365-88-2
Molecular Weight:
252.15
MDL number:
MFCD06201020
UNSPSC Code:
12352200
PubChem Substance ID:
57653383
NACRES:
NA.22

grade

technical

Assay

≥90% (AT)

form

liquid

reaction suitability

reagent type: cross-linking reagent

impurities

~5% 1-boc-pyrrolidine

functional group

Boc
amine
bromo

storage temp.

2-8°C

SMILES string

BrCCCCNC(OC(C)(C)C)=O

InChI

1S/C9H18BrNO2/c1-9(2,3)13-8(12)11-7-5-4-6-10/h4-7H2,1-3H3,(H,11,12)

InChI key

GKGFAEREWWZBKY-UHFFFAOYSA-N

Application

4-(Boc-amino)butyl bromide can be used:
  • For the synthesis of N-Boc-aminoalkoxyphenyl derivatives, precursor to pharmacophore elements for the treatment of glaucoma.
  • For the synthesis of various aloperine derivatives with potential application as anti-HIV agents.
  • For the modification of 4,5,6,7-tetrabromobenzotriazole (TBB) derivatives to generate improved CK2 inhibitors.

Other Notes

Building block for the synthesis of natural products and biologically active compounds.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H318

Precautionary Statements

P280 - P305 + P351 + P338

Hazard Classifications

Eye Dam. 1

Storage Class Code

10 - Combustible liquids

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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Identification of bivalent ligands with melatonin receptor agonist and fatty acid amide hydrolase (FAAH) inhibitory activity that exhibit ocular hypotensive effect in the rabbit.
Spadoni G, et al.
Journal of medicinal chemistry, 61(17), 7902-7916 (2018)
Structure Optimization of Aloperine Derivatives as HIV-1 Entry Inhibitors.
Dang Z, et al.
ACS Medicinal Chemistry Letters, 8(11), 1199-1203 (2017)
H. Ina et al.
The Journal of Organic Chemistry, 61, 1023 -1023 (1995)
Synthesis, biological activity and structural study of new benzotriazole-based protein kinase CK2 inhibitors.
Swider R, et al.
Royal Society of Chemistry Advances, 5(89), 72482-72494 (2015)
D.L. Selwood et al.
Journal of Medicinal Chemistry, 4, 78-78 (2001)

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