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302791

Sigma-Aldrich

Geranyl chloride

95%

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Synonym(s):
trans-1-Chloro-3,7-dimethyl-2,6-octadiene
Linear Formula:
(CH3)2C=CHCH2CH2C(CH3)=CHCH2Cl
CAS Number:
Molecular Weight:
172.69
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

95%

form

liquid

refractive index

n20/D 1.4808 (lit.)

bp

102-104 °C/12 mmHg (lit.)

density

0.931 g/mL at 25 °C (lit.)

SMILES string

C\C(C)=C\CC\C(C)=C\CCl

InChI

1S/C10H17Cl/c1-9(2)5-4-6-10(3)7-8-11/h5,7H,4,6,8H2,1-3H3/b10-7+

InChI key

WLAUCMCTKPXDIY-JXMROGBWSA-N

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1 of 4

This Item
329118187186412643
Geranyl chloride 95%

302791

Geranyl chloride

Geranyl bromide 95%

329118

Geranyl bromide

Cinnamyl chloride 95%

187186

Cinnamyl chloride

Geranylamine 90%

412643

Geranylamine

bp

102-104 °C/12 mmHg (lit.)

bp

101-102 °C/12 mmHg (lit.)

bp

108 °C/12 mmHg (lit.)

bp

105 °C/19 mmHg (lit.)

density

0.931 g/mL at 25 °C (lit.)

density

1.094 g/mL at 25 °C (lit.)

density

1.096 g/mL at 25 °C (lit.)

density

0.829 g/mL at 25 °C (lit.)

refractive index

n20/D 1.4808 (lit.)

refractive index

n20/D 1.504 (lit.)

refractive index

n20/D 1.584 (lit.)

refractive index

n20/D 1.476 (lit.)

form

liquid

form

liquid

form

liquid

form

liquid

General description

Geranyl chloride undergoes palladium-catalyzed cross-coupling reaction with aryl and alkenylgold(I) phosphanes to afford the α-substitution product.

Application

Geranyl chloride was used as starting reagent in the synthesis of:
  • C25 compound moenocinol
  • 2-methyl-6-geranylphenol
  • manoalide and seco-manoalide analogs

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

194.0 °F - closed cup

flash_point_c

90 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Toward elucidation of the inhibition mechanism of phospholipase A< sub> 2</sub> by manoalide: selectively modified amino acid residues by manoalide analogues.
Katsumura S, et al.
Bioorganic & Medicinal Chemistry Letters, 2(10), 1267-1268 (1992)
Preparation and oxidative polymerization of 2-methyl-6-geranylphenol.
Hyun SH, et al.
Polymer Bull., 18(4), 283-286 (1987)
A synthesis of moenocinol from isoprenoid precursors.
Bottger D and Welzel P.
Tetrahedron Letters, 24(47), 5201-5204 (1983)
Miguel Peña-López et al.
Organic & biomolecular chemistry, 10(8), 1686-1694 (2012-01-24)
Aryl and alkenylgold(I) phosphanes react regioselectively with allylic electrophiles such as cinnamyl and geranyl halides (bromide, chloride and acetates) under palladium catalysis in THF at 80 °C to afford the α-substitution product with moderate to high yields. When the reaction
Minju Lee et al.
Scientific reports, 8(1), 13945-13945 (2018-09-19)
We report a strategy for the human-like smelling of a rose scent utilizing olfactory receptor nanodisc (ND)-based bioelectronic nose devices. In this strategy, a floating electrode (FE)-based carbon nanotube (CNT) field effect transistor (FET) was functionalized with human olfactory receptor

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