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Merck
CN

459690

4-苄氧基-1-丁醇

97%

别名:

四亚甲基乙二醇单苄醚

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关于此项目

线性分子式:
C6H5CH2O(CH2)4OH
化学文摘社编号:
分子量:
180.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1944253
Assay:
97%
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Quality Segment

assay

97%

refractive index

n20/D 1.513 (lit.)

bp

216-256 °C (lit.)

density

1.025 g/mL at 25 °C (lit.)

functional group

ether, hydroxyl, phenyl

SMILES string

OCCCCOCc1ccccc1

InChI

1S/C11H16O2/c12-8-4-5-9-13-10-11-6-2-1-3-7-11/h1-3,6-7,12H,4-5,8-10H2

InChI key

TYROJDFHUXSBHC-UHFFFAOYSA-N

General description

4-Benzyloxy-1-butanol can be prepared starting from butane-1,4-diol.

Application

4-Benzyloxy-1-butanol may be used for the preparation of ethyl 6-benzyloxy-2-hexenoate, via Swern oxidation and Wadsworth-Emmons olefination. It may be used as starting reagent for the synthesis of 4-(benzyloxy)butanal.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

228.2 °F - closed cup

flash_point_c

109 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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The syntheses of tricyclic analogues of O 6-methylguanine.
Hammond DM, et al.
Organic & Biomolecular Chemistry, 1(23), 4166-4172 (2003)
Improved preparation of ?-hydroxy-a-amino acids: direct formation of sulfates by sulfuryl chloride.
Alonso M and Riera M.
Tetrahedron Asymmetry, 16(23), 3908-3912 (2005)



全球贸易项目编号

货号GTIN
459690-5ML04061837015212
459690-25ML04061837015205