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3-Buten-2-ol, benzoate, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90270-43-2

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90270-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90270-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,7 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90270-43:
(7*9)+(6*0)+(5*2)+(4*7)+(3*0)+(2*4)+(1*3)=112
112 % 10 = 2
So 90270-43-2 is a valid CAS Registry Number.

90270-43-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Buten-2-ol, 2-benzoate, (2S)-

1.2 Other means of identification

Product number -
Other names 3-Buten-2-ol, benzoate, (2S)-

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:90270-43-2 SDS

90270-43-2Relevant academic research and scientific papers

Catalytic asymmetric total synthesis of (S)-(-)-zearalenone, a novel lipoxygenase inhibitor

Baggelaar, Marc P.,Huang, Yange,Feringa, Ben L.,Dekker, Frank J.,Minnaard, Adriaan J.

, p. 5271 - 5274 (2013/09/02)

A catalytic asymmetric synthesis of (S)-(-)-zearalenone is reported using asymmetric allylic alkylation for the introduction of the stereocenter. (S)-(-)-Zearalenone turned out to be a novel lipoxygenase inhibitor.

PdII-catalyzed cascade reaction with 1,3-chirality transfer; Stereoselective synthesis of chiral nonracemic 2,2 ′ -THF-THF ring units

Uenishi, Junichi,Fujikura, Yuhei,Kawai, Nobuyuki

supporting information; experimental part, p. 2350 - 2353 (2011/06/25)

Chemical equations presented. A PdII-catalyzed cascade reaction of chiral nonracemic allylic alcohols possessing an internal mono- or diepoxide and a terminal alcohol provided a contiguous THF-THF ring unit stereospecifically. The cyclization t

Catalytic asymmetric carbong-carbon bond formation via allylic alkylations with organolithium compounds

Perez, Manuel,Fananas-Mastral, Martin,Bos, Pieter H.,Rudolph, Alena,Harutyunyan, Syuzanna R.,Feringa, Ben L.

experimental part, p. 377 - 381 (2012/01/06)

Carbon-carbon bond formation is the basis for the biogenesis of nature's essential molecules. Consequently, it lies at the heart of the chemical sciences. Chiral catalysts have been developed for asymmetric C-C bond formation to yield single enantiomers from several organometallic reagents. Remarkably, for extremely reactive organolithium compounds, which are among the most broadly used reagents in chemical synthesis, a general catalytic methodology for enantioselective C-C formation has proven elusive, until now. Here, we report a copper-based chiral catalytic system that allows carbon-carbon bond formation via allylic alkylation with alkyllithium reagents, with extremely high enantioselectivities and able to tolerate several functional groups. We have found that both the solvent used and the structure of the active chiral catalyst are the most critical factors in achieving successful asymmetric catalysis with alkyllithium reagents. The active form of the chiral catalyst has been identified through spectroscopic studies as a diphosphine copper monoalkyl species.

Copper catalyzed asymmetric synthesis of chiral allylic esters

Geurts, Koen,Fletcher, Stephen P.,Feringa, Ben L.

, p. 15572 - 15573 (2007/10/03)

The complex derived from Taniaphos ligand 4 and CuBr?Me2S catalyzes the asymmetric addition of Grignard reagents to 3-bromopropenyl esters 1 to provide allylic esters 2 in high yields and high chemio-, regio-, and enantioselectivities. The work demonstrates that allylic asymmetric alkylation (AAA) can be done on substrates bearing a heteroatom at the γ-position. The method is a practical route to chiral, nonracemic allylic alcohols. The use of functionalized substrates 1 or Grignard reagents leads to more complex products 2, which can be further manipulated as demonstrated in conversion to (S)-5-ethyl-2(5H)-furanone 6 and (S)-benzoic acid-cyclopent-2-enyl ester 7. Copyright

Kinetic resolution and unusual regioselectivity in palladium-catalyzed allylic alkylations with a chiral P,S ligand

Faller,Wilt, Jeremy C.,Parr, Jonathan

, p. 1301 - 1304 (2007/10/03)

Effective kinetic resolutions of acyclic allylic acetates and benzoates have been obtained using a palladium/(S)-BINAP(S) catalyst system. Unusually large preferences for the formation of branched alkylation products from 3-but-2-enyl and crotyl substrate

The effect of catechin derivatives on the enantioselectivity of lipase-catalyzed hydrolyses of alkynol benzoate esters

Nakamura, Kaoru,Takenaka, Keishi

, p. 415 - 422 (2007/10/03)

Polyphenols, such as (+)-catechin and pyrogallol could be used to enhance stereochemical control in the lipase-catalyzed hydrolysis of alkynol benzoate esters, leading to increased enantioselectivities in the kinetic resolution of alkynols with lipase Amano AH.

ANOMALOUS ADDITION OF TELLURIUM TETRACHLORIDE TO ALLYLIC ESTERS. SHORT SYNTHESIS OF TRANS-(2S,3S)-2,3-EPOXYBUTANE.

Engman

, p. 3977 - 3984 (2007/10/02)

The addition of tellurium to various allylic esters, alcohols, ethers, amides, and imino esters was studied. Allylic esters did not produce normal 1,2-chlorotelluration products, but the addition occurred 1,3 and was accompanied by a 1,2-migration of the acyloxy group. The examples include esters of allyl, alpha -methylallyl, alpha alpha -dimethylallyl, alpha -ethylallyl, methallyl, and (E)-crotyl alcohol, usually with benzoic acid but also with acetic, cinnamic, and crotonic acids.

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