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1-(m-tolyl)but-3-yn-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42250-02-2

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42250-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42250-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,5 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 42250-02:
(7*4)+(6*2)+(5*2)+(4*5)+(3*0)+(2*0)+(1*2)=72
72 % 10 = 2
So 42250-02-2 is a valid CAS Registry Number.

42250-02-2Relevant academic research and scientific papers

Electrophilic cyclization and intermolecular acetalation of 2-(4- hydroxybut-1-yn-1-yl)benzaldehydes: Synthesis of diiodinated diepoxydibenzo[c,k][1,9]dioxacyclohexadecines

Wang, Jia,Zhu, Hai-Tao,Chen, Si,Luan, Cheng,Xia, Yu,Shen, Yi,Li, Ying-Xiu,Hua, Yingxi,Liang, Yong-Min

, p. 10641 - 10649 (2017)

An expedient strategy for the preparation of diiodinated diepoxydibenzo[c,k][1,9]dioxacyclohexadecines from readily available 2-(4-hydroxybut-1-yn-1-yl)- benzaldehydes through electrophile-triggered tandem cyclization/ intermolecular acetalation sequence

One-Pot γ-Lactonization of Homopropargyl Alcohols via Intramolecular Ketene Trapping

Yamane, Daichi,Tanaka, Haruna,Hirata, Akihiro,Tamura, Yumiko,Takahashi, Daichi,Takahashi, Yusuke,Nagamitsu, Tohru,Ohtawa, Masaki

supporting information, p. 2831 - 2835 (2021/05/05)

A one-pot γ-lactonization of homopropargyl alcohols via an alkyne deprotonation/boronation/oxidation sequence has been developed. Oxidation of the generated alkynyl boronate affords the corresponding ketene intermediate, which is trapped by the adjacent hydroxy group to furnish the γ-lactone. We have optimized the conditions as well as examined the substrate scope and synthetic applications of this efficient one-pot lactonization.

Base-promoted direct synthesis of functionalized: N -arylindoles via the cascade reactions of allenic ketones with indoles

Li, Shengxiao,Wu, Xin-Xing,Chen, Shufeng

supporting information, p. 789 - 793 (2019/01/30)

A convenient Cs2CO3-promoted cascade benzannulation reaction of allenic ketones with indoles was achieved for the synthesis of functionalized N-arylindole derivatives under transition-metal-free conditions. A series of readily available starting materials can undergo the process successfully. It represents a practical method for the construction of N-arylindole scaffolds with high atom economy.

A bicyclization reaction with two molecular allenyl ketones and isocyanides: Synthesis of a lactone-containing azaspirocycle derivative

Yuan, Hongdong,Tang, Chongrong,Su, Shikuan,Cui, Lei,Jia, Xueshun,Li, Chunju,Li, Jian

supporting information, p. 7231 - 7234 (2019/07/02)

A novel bicyclization reaction of two molecular allenyl ketones and isocyanides has been disclosed. This strategy allows for the construction of structurally complex spirocyclic lactam-lactone systems in an efficient manner. This protocol also demonstrate

Gold-catalyzed regioselective synthesis of 2- and 3-alkynyl furans

Li, Yifan,Brand, Jonathan P.,Waser, Jerome

supporting information, p. 6743 - 6747 (2013/07/26)

Chemical Matching: C2- or C3-alkynylated furans were selectively synthesized by using gold catalysis. Direct C-H alkynylation of furans was achieved with C2 selectivity, and a domino cyclization/alkynylation process starting from allenes gave C3-alkynylat

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