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Oxirane, 2-ethynyl-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

221129-39-1

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221129-39-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 221129-39-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,1,2 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 221129-39:
(8*2)+(7*2)+(6*1)+(5*1)+(4*2)+(3*9)+(2*3)+(1*9)=91
91 % 10 = 1
So 221129-39-1 is a valid CAS Registry Number.

221129-39-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Ethynyl-3-phenyl-oxirane

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:221129-39-1 SDS

221129-39-1Upstream product

221129-39-1Relevant academic research and scientific papers

Metalation of 3-trimethylsilyl propargyl chloride: A stereoselective access to trans-propargylic oxiranes

Chemla, Fabrice,Bernard, Nicolas,Normant, Jean F.

, p. 75 - 78 (2007/10/03)

The metalation of 3-trimethylsilyl-1-chloroprop-2-yne and the subsequent reaction with aldehydes affords stereospecifically anti-chlorohydrins which give after treatment with potassium fluoride and NaOH propargylic epoxides with good to excellent yields.

Use of α-chlorosulfides in indium promoted C-C couplings: Easy entry into the stereoselective formation of epoxy alkynes

Engstrom, Gregory,Morelli, Meisha,Palomo, Carolyn,Mitzel, Thomas

, p. 5967 - 5970 (2007/10/03)

The use of α-chlorosulfide compounds to control stereoselectivity in indium promoted C-C couplings occurs smoothly at room temperature under aqueous and mixed aqueous/organic conditions. Use of the halide to control synlanti ratios simplifies the indium p

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