TERT-BUTYL PROPARGYL ETHER

CAS No.：16314-18-4

Important Notice

This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
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TERT-BUTYL PROPARGYL ETHER Basic information

Product Name:	TERT-BUTYL PROPARGYL ETHER
Synonyms:	TERT-BUTYL PROPARGYL ETHER;tert-Butyl propargyl ether,98%;tert-Butyl propargyl ether, 98% 5GR;1-Propyne,3-(1,1-dimethylethoxy)-;ert-Butylpropargylether;2-methyl-2-prop-2-ynoxypropane
CAS:	16314-18-4
MF:	C7H12O
MW:	112.17
EINECS:
Product Categories:
Mol File:	16314-18-4.mol

TERT-BUTYL PROPARGYL ETHER Chemical Properties

Boiling point	119℃
density	0.835
refractive index	1.417-1.419
Fp	20°(68°F)
storage temp.	Flammables area
form	Liquid
color	Clear light yellow

Safety Information

Hazard Codes	Xi-F
Risk Statements	36/37/38-11
Safety Statements	37/39-26-16
HazardClass	3
HS Code	29091990

MSDS Information

Provider	Language
ACROS	English

TERT-BUTYL PROPARGYL ETHER Usage And Synthesis

Chemical Properties

clear light yellow liquid

Uses

tert-Butyl Propargyl Ether is a versatile reactant with terminal alkyne group which was used in the preparation of ether and amine-functionalized internal vinylboronates by copper-NHC-catalyzed hydroboration of alkyne, propargyl alcohols and amines. tert-Butyl Propargyl Ether was also used in chemoselective and stereoselective preperation of vicinal diboronates via one-pot copper-catalyzed sequential hydroboration of alkyne in the presence of a chiral N-heterocyclic carbene ligand.

TERT-BUTYL PROPARGYL ETHER Preparation Products And Raw materials

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