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Merck
CN

302791

香叶基氯

95%

别名:

反式-1-氯-3,7-二甲基-2,6-辛二烯

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关于此项目

线性分子式:
(CH3)2C=CHCH2CH2C(CH3)=CHCH2Cl
化学文摘社编号:
分子量:
172.69
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
95%
Form:
liquid
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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.)

functional group

alkyl halide, chloro

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

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

存储类别

10 - Combustible liquids

wgk

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



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A synthesis of moenocinol from isoprenoid precursors.
Bottger D and Welzel P.
Tetrahedron Letters, 24(47), 5201-5204 (1983)
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)



全球贸易项目编号

货号GTIN
302791-1G04061837881053
302791-5G04061837881077