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2-Propenoic acid, 3-(phenylthio)-, methyl ester, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

49833-37-6

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49833-37-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49833-37-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,3 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 49833-37:
(7*4)+(6*9)+(5*8)+(4*3)+(3*3)+(2*3)+(1*7)=156
156 % 10 = 6
So 49833-37-6 is a valid CAS Registry Number.

49833-37-6Relevant academic research and scientific papers

Reaction of Arynes with Vinyl Sulfoxides: Highly Stereospecific Synthesis of ortho-Sulfinylaryl Vinyl Ethers

Li, Yuanming,Studer, Armido

, p. 666 - 669 (2017/02/10)

The reaction of in situ generated arynes with aryl vinyl sulfoxides provides ortho-arylsulfinylaryl vinyl ethers via aryne σ-bond insertion into the S-O-bond and concomitant stereospecific S-O-vinyl migration. The cascade allows preparing di- or trisubsti

Nickel(II) chloride-catalyzed regioselective hydrothiolation of alkynes

Ananikov, Valentine P.,Malyshev, Denis A.,Beletskaya, Irina P.,Aleksandrov, Grigory G.,Eremenko, Igor L.

, p. 1993 - 2001 (2007/10/03)

Regioselective Markovnikov-type addition of PhSH to alkynes (HC≡C-R) has been performed using easily available nickel complexes. The non-catalytic side reaction leading to anti-Markovnikov products was suppressed by addition of γ-terpinene to the catalyti

Preparation and Reactivity of β-(tri-n-butylstannyl)acrylates

Booth, Colin,Imanieh, Hussein,Quayle, Peter,Shui-Yu, Lu

, p. 413 - 416 (2007/10/02)

The reaction of heterofunctionalised vinyl stannanes with trichloroacetyl chloride occours without ipso-substitution, and provides easy access to a variety of β-(tri-n-butylstannyl)acrylates.

ALUMINIUM-CHLORIDE CATALYZED REACTION OF ALLYLIC SULFIDES WITH METHYL PROPIOLATE: A NOVEL ADDITION REACTION VIA AN IONIC SIGMATROPIC REARRANGEMENT

Hayakawa, Kenji,Kamikawaji, Yoshimasa,Kanematsu, Ken

, p. 2171 - 2174 (2007/10/02)

The aluminium-chloride catalyzed reaction of allylic sulfides with methyl propiolate resulted in the clean formation of novel 1:1 adducts via ionic sigmatropic rearrangements.

β-TRIBUTYLSTANNYLACRYLATES. STEREOSPECIFIC SYNTHESIS VIA CONJUGATE ADDITON OF TRIBUTYLSTANNYLCOPPER

Seitz, David E.,Lee, Shi-Hung

, p. 4909 - 4912 (2007/10/02)

The synthesis of cis- and trans-β-tributylstannylacrylates from conjugate addition of tributylstannylcopper to various β-substituted acrylates is shown to be a highly stereospecific reaction.Of four tributylstannylmetal reagents examined for this conversion, optimum results were obtained with tributylstannylcopper.

Ether substituted cyclopropanecarboxylic acids and esters

-

, (2008/06/13)

Novel esters of ether and thioether substituted cyclopropanecarboxylic acids, synthesis thereof, and intermediates therefor, such esters being useful as pesticides.

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