Cas 181120-06-9,Br(1-)*C12H17OS(1+)

181120-06-9

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Basic information

Product Name: Br^(1-)*C₁₂H₁₇OS⁽¹⁺⁾
Synonyms: Br^(1-)*C₁₂H₁₇OS⁽¹⁺⁾
CAS NO:181120-06-9
Molecular Formula:
Molecular Weight: 289.236
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Br^(1-)*C₁₂H₁₇OS⁽¹⁺⁾(CAS DataBase Reference)
NIST Chemistry Reference: Br^(1-)*C₁₂H₁₇OS⁽¹⁺⁾(181120-06-9)
EPA Substance Registry System: Br^(1-)*C₁₂H₁₇OS⁽¹⁺⁾(181120-06-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 181120-06-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 181120-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,1,2 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 181120-06:
(8*1)+(7*8)+(6*1)+(5*1)+(4*2)+(3*0)+(2*0)+(1*6)=89
89 % 10 = 9
So 181120-06-9 is a valid CAS Registry Number.

181120-06-9Upstream product

181120-06-9Downstream Products

181120-06-9Relevant academic research and scientific papers

Formal Asymmetric (4+1) Annulation Reaction between Sulfur Ylides and 1,3-Dienes

Rousseau, Olivier,Delaunay, Thierry,Dequirez, Geoffroy,Trieu-Van, Tran,Robeyns, Koen,Robiette, Rapha?l

, p. 12899 - 12902 (2015)

A highly enantioselective synthesis of functionalized cyclopentanoids by a formal asymmetric (4+1) annulation strategy was developed. The methodology consists of a stereoselective cyclopropanation reaction between chiral sulfur ylides and 1,3-dienes follo

Asymmetric sulfur-ylide-mediated formal [4+1]-annulation reaction: Scope and mechanism

Clergue, Sébastien,Rousseau, Olivier,Delaunay, Thierry,Dequirez, Geoffroy,Tran, Trieu-Van,Aakchioui, Soumia El,Barozzino-Consiglio, Gabriella,Robiette, Rapha?l

supporting information, p. 11417 - 11425 (2018/10/21)

A formal [4+1]-annulation strategy between sulfur ylides and 1,3-dienes was developed to afford functionalized cyclopentanoids. The process consists of a stereoselective cyclopropanation reaction followed, in situ, by a stereospecific MgI2-cata

Metal-free carbon-carbon cross-couplings between the ion pairs in sulfonium tetraphenylborates

Xu, Mei-Li,Huang, Wenhua

supporting information, p. 4230 - 4232 (2014/07/22)

A series of sulfonium tetraphenylborates can be readily prepared by the metathesis of sulfonium halides with sodium tetraphenylborates. After heating at 120-150 °C, the sulfonium tetraphenylborates can smoothly undergo the cross-couplings between the tetraphenylborate anions and the sulfonium cations in the absence of a metal catalyst. For carbonylmethyl-, benzyl-, and allylsulfoniums, the corresponding carbonylmethyl-phenyl, benzyl-phenyl, and allyl-phenyl cross-coupling products can be obtained in 22-76% yields. An interionic electron-transfer mechanism for this cross-coupling reaction is proposed.

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