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19170

3-丁烯-1-醇

purum, ≥98.0% (GC)

别名:

烯丙基甲醇

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关于此项目

线性分子式:
CH2=CHCH2CH2OH
化学文摘社编号:
627-27-0
分子量:
72.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329751827
EC Number:
210-991-3
Beilstein/REAXYS Number:
1633504
MDL number:
MFCD00002959
Assay:
≥98.0% (GC)
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grade

purum

Quality Level

100

assay

≥98.0% (GC)

refractive index

n20/D 1.421 (lit.), n20/D 1.422

bp

112-114 °C (lit.)

density

0.838 g/mL at 25 °C (lit.)

functional group

allyl, hydroxyl

SMILES string

OCCC=C

InChI

1S/C4H8O/c1-2-3-4-5/h2,5H,1,3-4H2

InChI key

ZSPTYLOMNJNZNG-UHFFFAOYSA-N

Application

3-Buten-1-ol was used as a starting reagent in asymmetric total synthesis of natural seimatopolide B. It was also used in the synthesis of catalytic bimetallic nanoparticles.

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pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

91.4 °F - closed cup

flash_point_c

33 °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
BCBP1862V

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Biologically programmed synthesis of bimetallic nanostructures.
Slocik JM and Naik RR.
Advanced Materials, 18(15), 1988-1992 (2006)
Alternating copolymers of functional alkenes with carbon monoxide.
Kacker S, et al.
Macromolecules, 29(18), 5852-5858 (1996)
Chada Raji Reddy et al.
Organic & biomolecular chemistry, 11(20), 3355-3364 (2013-04-09)
The asymmetric total synthesis of natural seimatopolide B along with its enantiomer is described starting from readily available 5-hexen-1-ol and 3-buten-1-ol. The key steps involved are Jacobson hydrolytic kinetic resolution, proline-catalyzed α-hydroxylation, Yamaguchi esterification and ring-closing metathesis. This asymmetric total

全球贸易项目编号

货号GTIN
19170-5ML04061837331299
19170-25ML04061838760265