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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
Assay:
99%
Form:
liquid
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vapor pressure

1.4 mmHg ( 20 °C)

Quality Level

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

SMILES string

C\C(C)=C\CO

InChI

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

InChI key

ASUAYTHWZCLXAN-UHFFFAOYSA-N

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

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


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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:

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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
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



全球贸易项目编号

货号GTIN
162353-500ML04061838746955
162353-5ML04061838746962
162353-100ML04061838746948