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Benzeneethanol, a-(phenylmethyl)-a-2-propenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138123-20-3

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138123-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138123-20-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,1,2 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 138123-20:
(8*1)+(7*3)+(6*8)+(5*1)+(4*2)+(3*3)+(2*2)+(1*0)=103
103 % 10 = 3
So 138123-20-3 is a valid CAS Registry Number.

138123-20-3SDS

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-benzyl-1-phenylpent-4-en-2-ol

1.2 Other means of identification

Product number -
Other names 2-Benzyl-1-phenyl-pent-4-en-2-ol

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:138123-20-3 SDS

138123-20-3Relevant academic research and scientific papers

Hydroxyl group-assisted palladium-catalyzed lactonization of homoallylic alcohols

Huang, Liangbin,Wang, Qian,Wu, Wanqing,Jiang, Huanfeng

, p. 561 - 566 (2014/03/21)

A convenient and highly efficient synthesis of α-methylene-γ- lactones through the palladium(II)-catalyzed lactonization of homoallylic alcohols with alkynamides has been reported. The hydroxyl group in the terminal olefins cooperates with the amide in alkynamides to promote the cyclization by suppressing the β-H elimination. This process provides a route to construct naturally occurring biologically multifunctional α-methylene-γ- lactones. The time has come to.i?lactonize: α-Methylene- γ-lactones are synthesized through the PdII-catalyzed lactonization of homoallylic alcohols with alkynamides. The hydroxyl group in the terminal olefins cooperates with the amide in alkynamides to promote the cyclization by suppressing the β-H elimination. This provides a route towards naturally occurring biologically multifunctional α-methylene- γ-lactones. Copyright

Enantioselective Pd(ii)-Pd(iv) catalysis utilizing a SPRIX ligand: Efficient construction of chiral 3-oxy-tetrahydrofurans

Takenaka, Kazuhiro,Dhage, Yogesh D.,Sasai, Hiroaki

supporting information, p. 11224 - 11226 (2013/11/19)

Novel enantioselective catalysis involving a Pd(ii)-Pd(iv) cycle was developed by utilizing a SPRIX ligand. Treatment of alkenyl alcohols with a catalytic amount of Pd-SPRIX and TfOH in the presence of PhI(OAc)2 gave optically active 3-oxy-tetr

General and convenient TsOH-induced allylboration of ketones

Matsuoka, Hiroaki,Kondo, Kazuhiro

experimental part, p. 2320 - 2321 (2009/09/06)

TsOH-induced allylation of various ketones with air- and moisture-stable potassium allyltrifluoroborate is described.

Lewis Acid-Promoted Addition of Allyl(cyclopentadienyl)iron(II) Dicarbonyl To Unactivated Ketones

Jiang, Songchun,Turos, Edward

, p. 4639 - 4642 (2007/10/02)

The Lewis acid-promoted addition of allyl(cyclopentadienyl)iron(II) dicarbonyl (1) to unactivated ketones provides zwitterionic iron-olefin complexes 5 as isolable salts.Treatment of these complexes with NaI in wet acetone affords homoallylic alcohols in

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