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Merck
CN

89171

6-(Boc-amino)hexyl bromide

≥97.0% (GC)

Synonym(s):

tert-Butyl N-(6-bromohexyl)carbamate

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About This Item

Empirical Formula (Hill Notation):
C11H22BrNO2
CAS Number:
142356-33-0
Molecular Weight:
280.20
NACRES:
NA.22
PubChem Substance ID:
57653330
UNSPSC Code:
12352200
MDL number:
MFCD06201019
Assay:
≥97.0% (GC)
Form:
liquid

Key Documents

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Product Name

6-(Boc-amino)hexyl bromide, ≥97.0% (GC)

InChI

1S/C11H22BrNO2/c1-11(2,3)15-10(14)13-9-7-5-4-6-8-12/h4-9H2,1-3H3,(H,13,14)

SMILES string

O=C(NCCCCCCBr)OC(C)(C)C

InChI key

NXQXVXILNVTMNA-UHFFFAOYSA-N

assay

≥97.0% (GC)

form

liquid

reaction suitability

reagent type: cross-linking reagent

refractive index

n20/D 1.473

density

1.192 g/mL at 20 °C (lit.)

functional group

Boc
amine
bromo

Quality Level

100

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Other Notes

Building block for preparing analogs of biologically active compounds

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H318

Hazard Classifications

Eye Dam. 1

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
BCBZ9386
BCBP8291V
BCBK1332V
BCBD3127V
BCBD3127

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D. Damour et al.
Bioorganic & Medicinal Chemistry Letters, 6, 1667 -1667 (1996)
T.H. Keller, R. Haener
Helvetica Chimica Acta, 76, 884-884 (1993)
Zaheer Ahmad et al.
Journal of biomaterials science. Polymer edition, 27(1), 40-54 (2015-10-23)
Tumor microenvironment-responsive nano drug delivery vehicles are gaining mounting attention in the field of biomedical sciences. The hypoxic response of the tumorous cells due to very low partial pressure of oxygen (some time less than 2.5 mm of Hg) in

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