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Key Documents

527513

Sigma-Aldrich

7-Bromo-1-heptene

≥97%

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About This Item

Linear Formula:
Br(CH2)5CH=CH2
CAS Number:
Molecular Weight:
177.08
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

≥97%

refractive index

n20/D 1.466 (lit.)

bp

27 °C/1 mmHg (lit.)

density

1.162 g/mL at 25 °C (lit.)

SMILES string

BrCCCCCC=C

InChI

1S/C7H13Br/c1-2-3-4-5-6-7-8/h2H,1,3-7H2

InChI key

GNYDYUQVALBGGZ-UHFFFAOYSA-N

General description

7-Bromo-1-heptene is a linear halogenated alkene.

Application

7-Bromo-1-heptene may be used to synthesize:
  • boc-L-2-amino-8-nonenoic acid (boc = tert-butyloxycarbonyl)
  • 9-hept-6-enyloxy-5-hydroxymethyl-2-isopropyl-1-methyl-1,4,5,6-tetrahydro-2H-benzo[e][1,4] diazocin-3-one
  • 8-hydroxy-15,15,15-trifluoro-1-pentadece

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

136.9 °F - closed cup

Flash Point(C)

58.3 °C - closed cup

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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Alan P Kozikowski et al.
ChemMedChem, 4(7), 1095-1105 (2009-04-28)
A series of benzolactam compounds were synthesized, some of which caused a concentration-dependent increase in sAPPalpha and decrease in Abeta production in the concentration range of 0.1-10 microM. Moreover, some compounds showed neuroprotective effects in the 10-20 microM range in
G H Stoll et al.
Journal of lipid research, 32(5), 843-857 (1991-05-01)
An analogue of the long-chain fatty acid salt, sodium stearate, was synthesized in which the hydrogen atoms at carbons 2, 3, and 18 were replaced by fluorine. The key step in the synthesis was the addition of 3-iodo-2,2,3,3-tetrafluoropropanoic acid amide
Norikazu Nishino et al.
Bioorganic & medicinal chemistry, 16(1), 437-445 (2007-09-29)
Inhibitors of histone deacetylases (HDACs) are a promising class of anticancer agents that effect gene regulation. To know the interaction of aliphatic cap groups with HDACs, cyclic tetrapeptide and bicyclic peptide disulfide hybrids were synthesized without aromatic ring in their

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