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Sigma-Aldrich

7-Bromo-1-heptene

≥97%

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About This Item

Fórmula lineal:
Br(CH2)5CH=CH2
Número de CAS:
4117-09-3
Peso molecular:
177.08
MDL number:
MFCD01631137
UNSPSC Code:
12352100
PubChem Substance ID:
24874623
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
GHS02,GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

136.9 °F - closed cup

flash_point_c

58.3 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

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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
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

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