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(2S,3R)-3-Methyl-2-phenylselanylmethyl-tetrahydro-furan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109065-98-7

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109065-98-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109065-98-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,0,6 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 109065-98:
(8*1)+(7*0)+(6*9)+(5*0)+(4*6)+(3*5)+(2*9)+(1*8)=127
127 % 10 = 7
So 109065-98-7 is a valid CAS Registry Number.

109065-98-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3R)-3-methyl-2-((phenylselanyl)methyl)tetrahydrofuran

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:109065-98-7 SDS

109065-98-7Downstream Products

109065-98-7Relevant academic research and scientific papers

Novel cyclization of unsaturated alcohols by phenyl selenocyanate in the presence of copper BIS(Trifluoromethanesulfonate)

Inoue, Hirofumi,Murata, Shizuaki

, p. 847 - 850 (2007/10/03)

Intramolecular oxyselenenylation of unsaturated alcohols by phenyl selenocyanate with copper bis(trifluoromethanesulfonate) proceeds stereoselectively to give cyclic ethers.

Stereoselective Cyclization of 4-Substituted 5-Hexen-1-ols and Related Compounds by Benzeneselenenyl Triflate

Inoue, Hirohumi,Murata, Shizuaki,Suzuki, Toshiyasu

, p. 901 - 910 (2007/10/02)

Oxyselenylation of 4-substituted 5-hexen-1-ols 1 with benzeneselenenyl trifluoromethanesulfonate proceeds by intramolecular exo cyclization stereoselectively to give 3-substituted trans- or cis-2-(phenylselenenylmethyl)tetrahydropyrans 3.Formation of the trans isomers is favored when the substituents contain alkyl or phenyl substituents in the 4-position, whereas the cis isomers predominate when the substituents are alkoxyalkyl, alkoxyl, acyl, and hydroxyl.The mechanism of the trans and cis stereoselectivity is explained by steric and electronic effects in the phenylseleniranium intermediates, 7 and 8. - Key Words: Oxyselenenylation / Benzeneselenenyl triflate / Selenium compounds / Trifluoromethanesulfonate / Alkenols

Stereoselectivity of Electrophile-Promoted Cyclizations of γ-Hydroxyalkenes. An Investigation of Carbohydrate-Derived and Model Substrates

Reitz, Allen B.,Nortey, Samuel O.,Maryanoff, Bruce E.,Liotta, Dennis,Robert, Monahan

, p. 4191 - 4202 (2007/10/02)

We have investigated cyclization reactions of γ-hydroxyalkenes bearing an alkoxy or alkyl substituent on the allylic carbon.A variety of electrophiles N-bromosuccinimide, N-iodosuccinimide, iodine, mercury(II) acetate, mercury(II) trifluoroacetate, mercu

CYCLIZATION OF OLEFINIC ALCOHOL BY BENZENESELENENYL TRIFLATE

Murata, Shizuaki,Suzuki, Toshiyasu

, p. 4297 - 4298 (2007/10/02)

Cyclization of 4-, 5-, and 6-hydroxyalkenes with benzeneselenenyl triflate afforded corresponding tetrahydrofurans and -pyrans.

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