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Merck
CN

527513

7-Bromo-1-heptene

≥97%

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About This Item

Linear Formula:
Br(CH2)5CH=CH2
CAS Number:
Molecular Weight:
177.08
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
≥97%
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InChI

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

SMILES string

BrCCCCCC=C

InChI key

GNYDYUQVALBGGZ-UHFFFAOYSA-N

assay

≥97%

refractive index

n20/D 1.466 (lit.)

bp

27 °C/1 mmHg (lit.)

density

1.162 g/mL at 25 °C (lit.)

functional group

alkyl halide, allyl, bromo

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

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

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

Regulatory Information

危险化学品
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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
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
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

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