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Merck
CN

162353

3-甲基-2-丁烯-1-醇

99%

别名:

3.3-二甲基烯丙醇, 异戊烯醇

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关于此项目

线性分子式:
(CH3)2C=CHCH2OH
化学文摘社编号:
分子量:
86.13
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39020334
UNSPSC Code:
12352100
EC Number:
209-141-4
MDL number:
Beilstein/REAXYS Number:
1633479
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产品名称

3-甲基-2-丁烯-1-醇, 99%

InChI key

ASUAYTHWZCLXAN-UHFFFAOYSA-N

InChI

1S/C5H10O/c1-5(2)3-4-6/h3,6H,4H2,1-2H3

SMILES string

C\C(C)=C\CO

vapor pressure

1.4 mmHg ( 20 °C)

assay

99%

form

liquid

expl. lim.

16.3 %

refractive index

n20/D 1.443 (lit.)

bp

140 °C (lit.)

density

0.848 g/mL at 25 °C (lit.)

functional group

hydroxyl

Quality Level

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Application

在通过Sharpless不对称环氧化反应不对称全合成(R)-(+)-和(S)-(-)-羟甲基甲基呋喃酮时,3-甲基-2-丁烯-1-醇被用作起始试剂

General description

3-甲基-2-丁烯-1-醇可与亚硝基羰基苯反应生成5-羟基-异恶唑烷。它常被用作芳香成分

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 1

flash_point_f

124.7 °F - closed cup

flash_point_c

51.5 °C - closed cup

ppe

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

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Anastasia Zerva et al.
Molecules (Basel, Switzerland), 23(9) (2018-09-22)
Feruloyl esterases (FAEs, E.C. 3.1.1.73) are biotechnologically important enzymes with several applications in ferulic acid production from biomass, but also in synthesis of hydroxycinnamic acid derivatives. The use of such biocatalysts in commercial processes can become feasible by their immobilization
Hong Liang et al.
Metabolic engineering, 65, 223-231 (2020-11-29)
Engineering microbes to utilize non-conventional substrates could create short and efficient pathways to convert substrate into product. In this study, we designed and constructed a two-step heterologous ethanol utilization pathway (EUP) in Escherichia coli by using acetaldehyde dehydrogenase (encoded by
Vijay Gnanadesikan et al.
Journal of the American Chemical Society, 130(25), 8089-8093 (2008-05-23)
An effective strategy has been developed for the efficient site-selective epoxidation of poylolefinic isoprenoid alcohols, based on the use of an internal control element for intramolecular reaction. The approach is illustrated by application to a series of polyisoprenoid alcohols (polyprenols)
Takeshi Bamba et al.
Journal of separation science, 32(15-16), 2699-2706 (2009-07-17)
Monolithic silica columns have very low back-pressures and offer several advantages over conventional columns packed with spherical particles, such as high separation efficiency and rapid analysis. In this review, we report the applicability of monolithic silica columns for the analysis
Branko Radetich et al.
Journal of the American Chemical Society, 124(11), 2430-2431 (2002-03-14)
A solution is reported to the classic unsolved problem of stereoselective synthesis of all-E oligoprenols, such as E-farnesylfarnesol, by a cationic coupling analogous to the biosynthetic pathway. The simplicity and efficacy of the method, which is outlined in Scheme 1

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