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Benzene, [(1E)-3-azido-1-butenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

233672-89-4

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233672-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 233672-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,3,6,7 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 233672-89:
(8*2)+(7*3)+(6*3)+(5*6)+(4*7)+(3*2)+(2*8)+(1*9)=144
144 % 10 = 4
So 233672-89-4 is a valid CAS Registry Number.

233672-89-4Relevant academic research and scientific papers

B(C6F5)3-catalyzed synthesis of benzylic azides

Wrigley, Michael S.,Barker, Timothy J.

, p. 1771 - 1776 (2017)

B(C6F5)3 was found to catalyze the reaction between trimethylsilyl azide and benzylic acetates. Secondary and tertiary benzylic acetates were competent substrates in this reaction providing the azide products in moderate t

Facile Direct Coupling Reactions of MOM-protected Benzylic Alcohols Using Aluminum Chloride

Bui, Tien Tan,Kim, Hee-Kwon

supporting information, p. 1195 - 1198 (2021/08/03)

MOM group is one of the most commonly used protecting groups for alcohols. This study describes novel direct functionalization of the MOM-protected benzylic alcohols. Preparation of allylic compounds from benzyl MOM ethers was successfully achieved by utilization of allyltrimethylsilane and AlCl3. In addition, direct azidation of benzyl MOM ethers using TMSN3 was successful carried out under AlCl3-mediated reaction conditions. These results demonstrate that this novel synthetic procedure is a promising approach to direct functionalization of MOM-protected alcohols including allylation and azidation.

VINYLOGOUS PHENETHYLAMINES AS NEUROTRANSMITTER RELEASERS

-

, (2017/12/02)

The disclosure provides monoamine neurotransmitter releaser and/or monoamine uptake inhibitor compounds having biogenic amine transporter activity but lacking substantial activity at 5-HT2 receptor subtypes. The phenethylamine or vinylogous phe

The biogenic amine transporter activity of vinylogous amphetamine analogs

Decker, Ann M.,Partilla, John S.,Baumann, Michael H.,Rothman, Richard B.,Blough, Bruce E.

, p. 1657 - 1663 (2016/08/24)

A series of vinylogous amphetamine analogs was synthesized and examined for their activity at biogenic amine transporters and serotonin-2 receptor (5-HT2) subtypes. (1S,3E)-1-Methyl-4-phenyl-but-3-enylamine (S-6) is a potent dual dopamine/serotonin (DA/5-HT) releaser with no activity at 5-HT2 receptors. This unique profile of actions suggests that analog S-6 is a viable lead compound for identifying new structural classes of DA/5-HT releasers with therapeutic benefit and reduced abuse liability.

Enantioselective, Stereodivergent Hydroazidation and Hydroamination of Allenes Catalyzed by Acyclic Diaminocarbene (ADC) Gold(I) Complexes

Khrakovsky, Dimitri A.,Tao, Chuanzhou,Johnson, Miles W.,Thornbury, Richard T.,Shevick, Sophia L.,Toste, F. Dean

supporting information, p. 6079 - 6083 (2016/05/19)

The gold-catalyzed enantioselective hydroazidation and hydroamination reactions of allenes are presented herein. ADC gold(I) catalysts derived from BINAM were critical for achieving high levels of enantioselectivity in both transformations. The sense of enantioinduction is reversed for the two different nucleophiles, allowing access to both enantiomers of the corresponding allylic amines using the same catalyst enantiomer. Chiral allylic azides and amines are obtained by enantioselective hydroazidation and hydroamination of allenes catalyzed by acyclic diaminocarbene gold(I) catalysts derived from BINAM. The sense of enantioinduction is reversed for the two different nucleophiles, allowing easy access to both enantiomers with a single catalyst enantiomer.

Copper-catalyzed direct transformation of secondary allylic and benzylic alcohols into azides and amides: An efficient utility of azide as a nitrogen source

Rokade, Balaji V.,Gadde, Karthik,Prabhu, Kandikere Ramaiah

, p. 2706 - 2717 (2015/04/27)

A mild and convenient method for the synthesis of amides has been explored by using secondary alcohols, Cu(ClO4)2·6H2O as a catalyst, and trimethylsilyl azide (TMSN3) as a nitrogen source in the presence of 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) at ambient temperature. This method has been successfully adapted to the preparation of azides directly from their corresponding alcohols and offers excellent chemoselectivity in the formation of ω-halo azides and the azidation of allylic alcohols in the presence of a benzyl alcohol moiety. In addition, this strategy provides an opportunity to synthesize azides that can serve as precursors to β-amino acids. A mild and convenient method for the synthesis of amides has been explored by using secondary alcohols, Cu(ClO4)2·6H2O as a catalyst, and trimethylsilyl azide (TMSN3) as a nitrogen source in the presence of 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) at ambient temperature. This method has also been adapted to the preparation of azides directly from their corresponding alcohols.

Chemoselective and direct functionalization of methyl benzyl ethers and unsymmetrical dibenzyl ethers by using iron trichloride

Sawama, Yoshinari,Goto, Ryota,Nagata, Saori,Shishido, Yuko,Monguchi, Yasunari,Sajiki, Hironao

, p. 2631 - 2636 (2014/03/21)

Methyl and benzyl ethers are widely utilized as protected alcohols due to their chemical stability, such as the low reactivity of the methoxy and benzyloxy groups as leaving groups under nucleophilic conditions. We have established the direct azidation of chemically stable methyl and benzyl ethers derived from secondary and tertiary benzyl alcohols. The present azidation chemoselectively proceeds at the secondary or tertiary benzylic positions of methyl benzyl ethers or unsymmetrical dibenzyl ethers and is also applicable to direct allylation, alkynylation, and cyanation reactions, as well as the azidation. The present methodologies provide not only a novel chemoselectivity but also the advantage of shortened synthetic steps, due to the direct process without the deprotection of the methyl and benzyl ethers. Ethers exchanged: Methyl and benzyl ethers are chemically stable and generally tolerant under nucleophilic substitution conditions. Iron-catalyzed direct functionalizations (e.g., azidation, allylation, alkynylation, and cyanation) of methyl and benzyl ethers derived from secondary and tertiary benzyl alcohols were established with excellent regioselectivities (see scheme; PG: protecting group; Bn: benzyl; Nu: nucleophile; TMS: trimethylsilyl). Copyright

Direct catalytic azidation of allylic alcohols

Rueping, Magnus,Vila, Carlos,Uria, Uxue

supporting information; experimental part, p. 768 - 771 (2012/03/26)

A direct catalytic azidation of primary, secondary, and tertiary allylic alcohols has been developed. This new azidation reaction affords the corresponding allylic azides in high to excellent yields and regioselectivities. The reaction provides straightforward access to allylic azides that are valuable intermediates in organic synthesis, including the preparation of primary amines or 1,2,3-triazole derivatives.

Iron-catalyzed chemoselective azidation of benzylic silyl ethers

Sawama, Yoshinari,Nagata, Saori,Yabe, Yuki,Morita, Kosuke,Monguchi, Yasunari,Sajiki, Hironao

supporting information, p. 16608 - 16611 (2013/03/13)

Azidation: Siloxy groups derived from secondary and tertiary benzyl alcohols can be transformed into azide groups at room temperature using TMSN3 in the presence of an iron catalyst (see scheme; TMS=trimethylsilyl). Secondary and tertiary benzy

Structure-based optimization of click-based histone deacetylase inhibitors

Hou, Jingli,Feng, Congran,Li, Zhonghua,Fang, Qinghong,Wang, Huihui,Gu, Guoxian,Shi, Yikang,Liu, Pi,Xu, Feng,Yin, Zheng,Shen, Jie,Wang, Peng

, p. 3190 - 3200 (2011/07/29)

Previously, we reported a click-chemistry based approach to the synthesis of a novel class of histone deacetylase (HDAC) inhibitors [1]. The lead compound NSC746457 was found to be as potent as SAHA (Vorinostat). Further optimization of NSC746457 by using

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