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关于此项目
线性分子式:
C6H5CH2OCH2CH=CHCH2OH
化学文摘社编号:
分子量:
178.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3605116
Assay:
≥95%
Form:
liquid
Quality Level
assay
≥95%
form
liquid
refractive index
n20/D 1.534 (lit.)
bp
105-108 °C/0.1 mmHg (lit.)
density
1.058 g/mL at 25 °C (lit.)
functional group
ether, hydroxyl, phenyl
storage temp.
2-8°C
SMILES string
OC\C=C/COCc1ccccc1
InChI
1S/C11H14O2/c12-8-4-5-9-13-10-11-6-2-1-3-7-11/h1-7,12H,8-10H2/b5-4-
InChI key
CGLJRLXTVXHOLX-PLNGDYQASA-N
Application
cis-4-Benzyloxy-2-buten-1-ol may be used in the synthesis of cis-4-benzyloxybuten-2-ylamine via Mitsunobu reaction.
signalword
Warning
hcodes
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
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Synthesis of Novel 3-Substituted Pyrrolo[2,3-b]quinoxalines via an Intramolecular Heck Reaction on an Aminoquinoxaline Scaffold.
Jie Jack Li
The Journal of organic chemistry, 64(22), 8425-8427 (2001-10-25)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 359599-5ML | 04061837323645 |
