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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
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
此项目有
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Concanavalin A (ConA) kills the procyclic (insect) form of Trypanosoma brucei by binding to its major surface glycoprotein, procyclin. We previously isolated a mutant cell line, ConA 1-1, that is less agglutinated and more resistant to ConA killing than are
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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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 162353-100ML | 04061838746948 |
| 162353-500ML | 04061838746955 |
| 162353-5ML | 04061838746962 |


