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β-Tributylstannylpropionaldehyde is an organotin compound with the chemical formula C15H30OSn. It is a colorless liquid that is soluble in organic solvents. β-tributylstannylpropionaldehyde is primarily used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds through the Stille coupling reaction, a type of cross-coupling reaction. It is also employed as a reducing agent in various chemical transformations. Due to its reactivity and the potential health and environmental risks associated with organotin compounds, it is important to handle β-tributylstannylpropionaldehyde with care, following proper safety protocols.

82994-41-0

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82994-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82994-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,9 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82994-41:
(7*8)+(6*2)+(5*9)+(4*9)+(3*4)+(2*4)+(1*1)=170
170 % 10 = 0
So 82994-41-0 is a valid CAS Registry Number.

82994-41-0SDS

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 (E)-3-hydroxy-1-tributylstannyl-1-propene

1.2 Other means of identification

Product number -
Other names (E)-3-(tri-n-butylstannyl)-2-propen-1-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:82994-41-0 SDS

82994-41-0Downstream Products

82994-41-0Relevant academic research and scientific papers

Synthesis of Optically Active N -(4-Hydroxynon-2-enyl)pyrrolidines: Key Building Blocks in the Total Synthesis of Streptomyces coelicolor Butanolide 5 (SCB-5) and Virginiae Butanolide A (VB-A)

Donges, Jonas,Hofmann, Sandra,Walter, Johannes C.,Reichertz, Julia,Brüggemann, Moritz,Frank, Andrea,Nubbemeyer, Udo

, p. 2632 - 2642 (2021)

Starting from 5-methylhexanal and (S)-configured N -propargylprolinol ethers, coupling delivered N -(4-hydroxynon-2-ynyl)prolinol derivatives as mixtures of C4 diastereomers. Resolution of the epimers succeeded after introduction of an (R)-mandelic ester derivative and subsequent HPLC separation. Alternatively, suitable oxidation gave the corresponding alkynyl ketone. Midland reagent controlled diastereoselective reduction afforded a defined configured propargyl alcohol with high selectivity. LiAlH 4reduction and Mosher analyses of the allyl alcohols enabled structure elucidation. The suitably protected products are used as key intermediates in enantioselective Streptomyces γ-butyrolactone signaling molecule total syntheses.

Substituted Tetraethynylethylene–Tetravinylethylene Hybrids

Connor, Kieran P. E.,Horvath, Kelsey L.,Magann, Nicholas L.,Sherburn, Michael S.,Sowden, Madison J.,Westley, Erin

supporting information, p. 977 - 986 (2022/02/03)

A general synthetic approach to molecular structures that are hybrids of tetraethynylethylene (TEE) and tetravinylethylene (TVE) is reported. The synthesis permits the controlled preparation of many previously inaccessible structures, including examples w

PROBE FOR DETECTING CARBAPENEM-RESISTANT BACTERIA AND USE THEREOF

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Paragraph 0085; 0099; 0100, (2021/09/10)

The present disclosure relates to a compound represented by Chemical Formula 1, a probe for detecting antibiotic-resistant bacteria, which includes the compound, a composition containing the compound, a kit including the compound and a method for detectin

Synthesis of (Z)-alkene-containing linear conjugated dienyl homoallylic alcohols by a palladium-catalyzed three-component reaction

Horino, Yoshikazu,Sakamoto, Juri,Murakami, Miki,Sugata, Miki

supporting information, p. 1323 - 1327 (2020/08/21)

A synthesis of (Z)-alkene-containing linear conjugated dienyl homoallylic alcohols by using a palladium-catalyzed three-component reaction has been developed. This method shows good functional-group compatibility and generality, with high diastereoselectivity. Additionally, in many cases, the present method controls the alkene stereochemistry of the newly formed C-C bond and overcomes the inherent preference for (E)-alkene formation, giving (Z, E)- and (Z, Z)-products.

Total Synthesis of Lajollamycin B

Nishimaru, Tatsuya,Eto, Kohei,Komine, Keita,Ishihara, Jun,Hatakeyama, Susumi

, p. 7927 - 7934 (2019/05/27)

The first total synthesis of lajollamycin B, a structurally novel nitro-tetraene spiro-β-lactone/γ-lactone antibiotic, is described. The convergent synthesis involves the construction of the C8′–C11′ nitrodienylstannane and its coupling with the segment prepared from the C1′–C7′ ω-iodoheptadienoic acid and the right-hand heterocyclic fragment, which has been utilized for our previous syntheses of oxazolomycin A. The revision of the geometry of the terminal Δ10′, 11′-double bond from E to Z is also described for the structure of natural lajollamycin B.

Synthesis of the C1-C12 Fragment of Calyculin C

Konstantinova, Olga V.,Koskinen, Ari M.P.

, p. 285 - 295 (2019/01/04)

Calyculins are a class of highly cytotoxic metabolites originally isolated from the marine sponge Discodermia calyx. To date, a total of twelve different calyculins (A-J) and calyculinamides (A, B and F) have been described, the most abundant (in D. calyx

Total Synthesis of the Marine Macrolide Amphidinolide F

Ferrié, Laurent,Fenneteau, Johan,Figadère, Bruno

supporting information, p. 3192 - 3196 (2018/06/11)

A new and efficient convergent approach toward the synthesis of amphidinolide F is described through the assembly of three fragments. The two trans-tetrahydrofurans were built by a diastereoselective C-glycosylation with titanium enolate of bulky N-acetyloxazolidinethiones. The side chain was inserted by a Liebeskind-Srogl cross-coupling reaction. A sulfone condensation/desulfonylation sequence, a Stille cross-coupling, and a macrolactonization were applied to connect the fragments.

Versatile synthetic route to carbocyclic N-Acetylneuraminic acid and its derivatives

Mohan, Sankar,Thompson, John R.,Pinto, B. Mario,Bennet, Andrew J.

, p. 5213 - 5221 (2018/05/29)

Sialic acid (N-acetylneuraminic acid) is a carbohydrate that possess a nine carbon backbone, and it is often found at the termini of glycoconjugates in biological systems. Because of this prominence many syntheses have reported routes to sialic acid and m

SYNTHESIS OF DISORAZOLES AND ANALOGS THEREOF AS POTENT ANTICANCER AGENTS

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Page/Page column 89; 116, (2019/01/11)

In one aspect, the present disclosure provides disorazole analogs of the formula: Formula (I) wherein the variables are as defined herein. In another aspect, the present disclosure also provides methods of preparing the compounds disclosed herein. In another aspect, the present disclosure also provides pharmaceutical compositions and methods of use of the compounds disclosed herein. Additionally, drug conjugates with cell targeting moieties of the compounds are also provided.

Total Syntheses of Disorazoles A1 and B1 and Full Structural Elucidation of Disorazole B1

Nicolaou,Bellavance, Gabriel,Buchman, Marek,Pulukuri, Kiran Kumar

supporting information, p. 15636 - 15639 (2017/11/14)

Described herein are the first total syntheses of naturally occurring antitumor agents disorazoles A1 and B1 and the full structural assignment of the latter. The syntheses were achieved through convergent strategies employing enantioselective constructions of the required building blocks, including a novel Sharpless epoxidation/enzymatic kinetic resolution of stannane-containing substrates that led selectively to both enantiomeric forms of an epoxy vinyl stannane, and a series of coupling reactions, including a Wittig reaction, a Suzuki coupling, a Stille coupling, a Yamaguchi esterification and a Yamaguchi macrolactonization.

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