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Merck
CN

118559

Sigma-Aldrich

1,5-己二烯-3-醇

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线性分子式:
H2C=CHCH2CH(OH)CH=CH2
CAS号:
分子量:
98.14
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

折射率

n20/D 1.448 (lit.)

密度

0.878 g/mL at 25 °C (lit.)

SMILES字符串

OC(CC=C)C=C

InChI

1S/C6H10O/c1-3-5-6(7)4-2/h3-4,6-7H,1-2,5H2

InChI key

SZYLTIUVWARXOO-UHFFFAOYSA-N

一般描述

1,5-Hexadien-3-ol is the starting reagent for the enantioselective synthesis of (+)-rogioloxepane A. It undergoes Sharpless kinetic resolution and ring-closing metathesis to yield nine membered oxocene.

应用

1,5-Hexadien-3-ol was used in the synthesis of (+)-obtusenyne.

象形图

Flame

警示用语:

Warning

危险声明

危险分类

Flam. Liq. 3

WGK

WGK 3

闪点(°F)

84.2 °F

闪点(°C)

29 °C

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品

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Michael T Crimmins et al.
Journal of the American Chemical Society, 125(25), 7592-7595 (2003-06-19)
A total synthesis of the laurencia metabolite (+)-obtusenyne has been completed. The key steps include a Sharpless kinetic resolution and an asymmetric glycolate alkylation to establish the stereogenic centers adjacent to the ether linkage and a ring-closing metathesis reaction to
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