Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

Safety Information

17354

Sigma-Aldrich

2-(Boc-amino)ethyl bromide

≥97.0% (GC)

Synonym(s):

N-Boc-2-bromoethyl-amine, tert-Butyl N-(2-bromoethyl)carbamate

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
BrCH2CH2NHCO2C(CH3)3
CAS Number:
39684-80-5
Molecular Weight:
224.10
Beilstein:
2325117
MDL number:
MFCD02683428
UNSPSC Code:
12352101
PubChem Substance ID:
57647641
NACRES:
NA.22

Quality Level

200

Assay

≥97.0% (GC)

reaction suitability

reagent type: cross-linking reagent

mp

30-32 °C (lit.)

functional group

Boc
amine
bromo

shipped in

wet ice

storage temp.

−20°C

SMILES string

BrCCNC(OC(C)(C)C)=O

InChI

1S/C7H14BrNO2/c1-7(2,3)11-6(10)9-5-4-8/h4-5H2,1-3H3,(H,9,10)

InChI key

TZRQZPMQUXEZMC-UHFFFAOYSA-N

Related Categories

General description

2-(Boc-amino)ethyl bromide is used in organic synthesis to introduce Boc-protective group and enable the synthesis of various compounds like peptides.

Other Notes

Building block for preparing fluorinated spacers having nucleophilic and electrophilic termini; synthesis of a biphenyl linker

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

17354-BULK:
17354-5G:
17354-VAR:
17354-INTR:
17354-1G:

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCBK0278V
1371897V
1371897
1369927
BCBJ2721V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

L. Chen et al.
Tetrahedron Letters, 39, 3627-3627 (1998)
Convergent Synthesis and Diversity of Amino Acid Based Dendrimers
Arwin J B, et al.
European Journal of Organic Chemistry, 1903-1915 (2001)
P. Mougenot et al.
The Journal of Organic Chemistry, 61, 408-408 (1996)
Jinping Cheng et al.
International journal of nanomedicine, 6, 2007-2021 (2011-10-07)
Carbon nanotubes have shown broad potential in biomedical applications, given their unique mechanical, optical, and chemical properties. In this pilot study, carbon nanotubes have been explored as multimodal drug delivery vectors that facilitate antiangiogenic therapy in zebrafish embryos. Three different
Marina Marinović et al.
Molecules (Basel, Switzerland), 25(19) (2020-09-27)
Harmicines represent hybrid compounds composed of β-carboline alkaloid harmine and cinnamic acid derivatives (CADs). In this paper we report the synthesis of amide-type harmicines and the evaluation of their biological activity. N-harmicines 5a-f and O-harmicines 6a-h were prepared by a

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service