跳转至内容
Merck
CN

162353

Sigma-Aldrich

3-甲基-2-丁烯-1-醇

99%

别名:

3.3-二甲基烯丙醇, 异戊烯醇

登录查看公司和协议定价

选择尺寸


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
Beilstein:
1633479
EC 号:
MDL编号:
UNSPSC代码:
12352100
eCl@ss:
39020334
PubChem化学物质编号:
NACRES:
NA.22
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

蒸汽压

1.4 mmHg ( 20 °C)

质量水平

方案

99%

表单

liquid

expl. lim.

16.3 %

折射率

n20/D 1.443 (lit.)

沸点

140 °C (lit.)

密度

0.848 g/mL at 25 °C (lit.)

官能团

hydroxyl

SMILES字符串

C\C(C)=C\CO

InChI

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

InChI key

ASUAYTHWZCLXAN-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

一般描述

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

应用

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

警示用语:

Danger

危险分类

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

靶器官

Respiratory system

储存分类代码

3 - Flammable liquids

WGK

WGK 1

闪点(°F)

124.7 °F - closed cup

闪点(°C)

51.5 °C - closed cup

个人防护装备

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

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

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
Huawei Liu et al.
Chirality, 18(4), 223-226 (2006-03-08)
The asymmetric total syntheses of (R)-(+)- and (S)-(-)-umbelactone were achieved by using the Sharpless asymmetric epoxidation reaction to generate the stereogenic center and a ring-closing metathesis (RCM) for the formation of the lactone structure. Starting from 3-methyl-2-buten-1-ol, the asymmetric total
Dusan Hesek et al.
Journal of the American Chemical Society, 134(33), 13881-13888 (2012-08-07)
We describe a practical, multigram synthesis of (2Z,6Z,10Z,14Z,18E,22E)-3,7,11,15,19,23,27-heptamethyl-2,6,10,14,18,22,26-octacosaheptaen-1-ol [(Z(4),E(2),ω)-heptaprenol, 4] using the nerol-derived sulfone 8 as the key intermediate. Sulfone 8 is prepared by the literature route and is converted in five additional steps (18% yield from 8) to (Z(4),E(2),ω)-heptaprenol
Teris A van Beek
Journal of chromatography. A, 967(1), 21-55 (2002-09-11)
The chemical analysis and quality control of Ginkgo leaves and extracts is reviewed. Important constituents present in the medicinally used leaves are the terpene trilactones, i.e., ginkgolides A, B, C, J and bilobalide, many flavonol glycosides, biflavones, proanthocyanidins, alkylphenols, simple
Charla A Centrone et al.
Bioorganic & medicinal chemistry, 12(21), 5495-5503 (2004-10-07)
Mycobacteria biosynthesize a cell wall structure that is rich in polysaccharides containing arabinofuranose residues. The source of these arabinofuranose residues is decaprenolphosphoarabinose (1), the donor substrate for mycobacterial arabinosyltransferases. We have previously demonstrated that an analog of 1, C-phosphonate 7

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持