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6712-35-2

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6712-35-2 Usage

Synthesis Reference(s)

Tetrahedron Letters, 34, p. 15, 1993 DOI: 10.1016/S0040-4039(00)60046-1

Check Digit Verification of cas no

The CAS Registry Mumber 6712-35-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,1 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6712-35:
(6*6)+(5*7)+(4*1)+(3*2)+(2*3)+(1*5)=92
92 % 10 = 2
So 6712-35-2 is a valid CAS Registry Number.

6712-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-2-phenylpent-4-yn-2-ol

1.2 Other means of identification

Product number -
Other names 2-Phenyl-pent-4-in-2-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:6712-35-2 SDS

6712-35-2Relevant academic research and scientific papers

Indium-mediated allylation of carbonyl compounds in deep eutectic solvents

González-Gallardo, Nerea,Saavedra, Beatriz,Guillena, Gabriela,Ramón, Diego J.

, (2021/08/26)

This study describes, for the first time, the in situ generation of indium organometallic reagents in environmentally friendly deep eutectic solvents (DESs). The allylation process of different carbonyl compounds is achieved mediated by indium metal and u

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.

A Mechanochemical Zinc-Mediated Barbier-Type Allylation Reaction under Ball-Milling Conditions

Yin, JieXiang,Stark, Roderick T.,Fallis, Ian A.,Browne, Duncan L.

, p. 2347 - 2354 (2020/02/04)

A ball-milling-enabled zinc-mediated Barbier-type allylation reaction is reported. Notably, running the reaction in this manner renders it effective irrespective of the initial morphology of the zinc metal. The process is operationally simple, does not re

One-pot, regioselective synthesis of homopropargyl alcohols using pro-pargyl bromide and carbonyl compound by the mg-mediated reaction under solvent-free conditions

Devaramani, Samrat,Li, Shunxi,Ma, Xiaofang,Xu, Daqian,Zhao, Guohu

supporting information, p. 438 - 442 (2020/04/21)

The elimination of volatile organic solvents in organic synthesis is the most important goal in “Green” chemistry. We report a simple, efficient and facile method for the addition of progargyl bromide to carbonyl compounds using Mg metal as a mediator under solvent-free conditions which could regioselectively generate homopropargyl alcohols efficiently in good to excellent yields. The procedure has advantages such as short reaction time, operationally simple, excellent product yields, high regioselectivity and organic solvent-free.

Synthesis of Cyclopropanes via 1,3-migration of acyloxy groups triggered by formation of α-Imino Rhodium Carbenes

Xu, Ze-Feng,Liu, Jincheng,Chang, Xin,Chen, Tao,Xu, Huaping,Duan, Shengguo,Li, Chuan-Ying

supporting information, p. 5163 - 5169 (2020/07/16)

A novel and highly efficient synthetic approach to cyclopropanes was realized via 1,3-migration of acyloxy groups triggered by α-imino rhodium carbenes. Excellent chemoselectivity ensured broad compatibility of common functional groups. Merits such as readily available substrates, mild reaction conditions, and time-saving processes qualified this transformation as an attractive alternative strategy to synthesize multifunctionalized cyclopropanes. Primary investigations and discussion on the mechanism are presented.

Palladium-Catalyzed One-Pot Conversion of Aldehydes and Ketones into 4-Substituted Homopropargyl Alcohols and 5-En-3-yn-1-ols ?

Umana, Christian A.,Cabezas, Jorge A.

, p. 9505 - 9514 (2017/09/23)

Sequential treatment of 2,3-dichloropropene with magnesium and n-BuLi generated the equivalent of 1,3-dilithiopropyne, which adds regiospecifically to aldehydes and ketones to produce homopropargyl alcohols. The lithium acetylide intermediate formed in this protocol can be further reacted with aromatic and vinyl halides, under palladium catalysis, to produce 4-substituted homopropargyl alcohols and 5-en-3-yn-1-ols, respectively, in one-pot with good overall yields.

TBAI/K2S2O8 Initiated Radical Cyclization to Synthesize β- Arylsulfonyl Naphthalenes from Homopropargylic Alcohols and Sulfonyl Hydrazides

Yang, Xiaodong,Zhao, Lianbiao,Yuan, Bingxiang,Qi, Zhenjie,Yan, Rulong

supporting information, p. 3248 - 3253 (2017/09/06)

A metal-free radical addition method for the synthesis of β-arylsulfonyl naphthalenes with homopropargylic alcohols and sulfonyl hydrazides has been developed. In this reaction, sulfonyl hydrazide is employed as the source of sulfonyl radical to produce the desired sulfone directly. There is the first example for homopropargylic alcohol through direct intramolecular addition of vinyl radical to arenes with sulfonyl radical, which is initiated by the TBAI/K2S2O8 reaction system and generates the desired products in moderate yields. (Figure presented.).

Re-engineering of PIP3-antagonist triazole PITENIN's chemical scaffold: Development of novel antifungal leads

Pulya, Sravani,Kommagalla, Yadagiri,Sant, Duhita G.,Jorwekar, Shweta U.,Tupe, Santosh G.,Deshpande, Mukund V.,Ramana, Chepuri V.

, p. 11691 - 11701 (2016/02/09)

A novel 4-(1-phenyl-1-hydroxyethyl)-1-(o-hydroxyphenyl)-1H-1,2,3-triazole was designed by integrating the structural features of triazole PITENIN anticancer agents and the azole class of antifungal drugs. A two-step protocol comprising the Barbier proparg

Zinc Amide Catalyzed Regioselective Allenylation and Propargylation of Ketones with Allenyl Boronate

Yamashita, Yasuhiro,Cui, Yi,Xie, Peizhong,Kobayashi, Shu

supporting information, p. 6042 - 6045 (2016/01/09)

Zinc amide catalyzed, regioselective allenylation and propargylation of ketones with allenyl boronate is reported. Tertiary allenyl and homopropargyl alcohols were obtained, respectively, in high selectivities, from the same starting materials, simply by changing the reaction conditions. The substrate scope was wide. Mechanistic studies suggest that the reactions are controlled under kinetic and thermodynamic conditions.

NOVEL 1,2,3 TRIAZOLE ANTIFUNGAL AGENTS AND PREPARATION THEREOF

-

Page/Page column 12, (2016/06/06)

The present application relates to 1,4-disubstituted 1,2,3-Triazole antifungal agents of the formula (I) wherein, R1 is halogens such as fluorine, chlorine or bromine, CF3, alkyl; R2 is alkyl or hydrogen; R3 is halogen selected from fluorine, chlorine or bromine; and n is 0 or 1. The application further relates to the synthesis of said compounds, to fungicidal compositions containing said compounds and to their use in a method for treating fungal infections.

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