Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
(CH3)3SiCH2CH2OCH2Cl
CAS Number:
Molecular Weight:
166.72
UNSPSC Code:
12352101
NACRES:
NA.22
PubChem Substance ID:
EC Number:
278-483-4
Beilstein/REAXYS Number:
3587289
MDL number:
Form:
liquid
grade
technical grade
Quality Level
form
liquid
refractive index
n20/D 1.435 (lit.)
bp
170-172 °C (lit.), 57-59 °C/8 mmHg (lit.)
density
0.942 g/mL at 25 °C (lit.)
functional group
chloro, ether
storage temp.
−20°C
SMILES string
C[Si](C)(C)CCOCCl
InChI
1S/C6H15ClOSi/c1-9(2,3)5-4-8-6-7/h4-6H2,1-3H3
InChI key
BPXKZEMBEZGUAH-UHFFFAOYSA-N
General description
Learn More at the Professor and Product Portal of Professor Bruce Lipshutz.
Application
Phenol protecting group in the synthesis of laterifluorones.
Used to prepare a SEM-ether which was, in turn, removed with BBr3 and cyclized to a benzo-oxapane.
Features and Benefits
Convenient hydroxyl-protecting reagent. SEM-ethers are stable over a wide pH range, and can be selectively cleaved with fluoride ion under mild aprotic conditions.
Disclaimer
Supply conditions do not apply to the regions and states of Brazil: North, Northeast, Mato Grosso do Sul, Mato Grosso, and Rio Grande do Sul.
Still not finding the right product?
Explore all of our products under 2-(Trimethylsilyl)ethoxymethyl chloride
signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 3 - Skin Corr. 1B
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
114.8 °F - closed cup
flash_point_c
46 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Related Content
Designer surfactants enable diverse transformations like Suzuki-Miyaura, Olefin Metathesis, and 1,4-Addition to Enones in water by Prof. Bruce Lipshutz.
Tetrahedron Letters, 36, 1683-1683 (1995)
K C Nicolaou et al.
Journal of the American Chemical Society, 126(17), 5493-5501 (2004-04-29)
The total synthesis of 1-O-methyllateriflorone (2) is described. The construction of the cage-like domain of the molecule involved a biomimetic Claisen/Diels-Alder cascade, whereas the novel spiroxalactone framework was generated by an intramolecular Michael reaction within precursor 16a involving the carboxylate
The Journal of Organic Chemistry, 55, 5180-5180 (1990)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 238902-5G | 04061837522215 |
| 238902-100G | 04061837522185 |
| 238902-1G | 04061837522208 |
| 238902-25G | 04061838787224 |

