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1-(Benzyloxy)-4-(cyclopropylMethyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

868699-62-1

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868699-62-1 Usage

Structure

Benzene derivative with a benzyloxy group and a cyclopropylmethyl group attached to the benzene ring

Potential applications

a. Organic synthesis
b. Pharmaceutical research

Use

Building block in the synthesis of various organic compounds and pharmaceutical agents

Cyclopropylmethyl group

Confers specific biological and pharmacological properties

Target for

Drug discovery and development

Versatility

Applicable in various fields of chemistry and pharmaceutical research

Check Digit Verification of cas no

The CAS Registry Mumber 868699-62-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,6,9 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 868699-62:
(8*8)+(7*6)+(6*8)+(5*6)+(4*9)+(3*9)+(2*6)+(1*2)=261
261 % 10 = 1
So 868699-62-1 is a valid CAS Registry Number.

868699-62-1Downstream Products

868699-62-1Relevant academic research and scientific papers

Photoredox/Nickel Dual Catalysis Enables the Synthesis of Alkyl Cyclopropanes via C(sp3)-C(sp3) Cross Electrophile Coupling of Unactivated Alkyl Electrophiles

Dey, Purusattam,Jana, Sayan K.,Maiti, Mamata,Maji, Biplab

supporting information, p. 1298 - 1302 (2022/02/25)

A facile synthesis of mono-, 1,1- and 1,2-disubstituted cyclopropanes via visible light-mediated photoredox/nickel dual catalysis is demonstrated. The challenging intramolecular C(sp3)-C(sp3) cross-electrophile coupling of readily available unactivated 1,3-dialkyl electrophiles was performed under mild conditions that allowed traditionally reactive functional groups to be included. Mechanistic inspection and control experiments revealed the importance of dual catalysis and that the reaction proceeds via a stepwise oxidative addition followed by an intramolecular SN2 reaction.

An efficient synthesis of aryloxyphenyl cyclopropyl methanones: A new class of anti-mycobacterial agents

Dwivedi, Namrata,Tewari, Neetu,Tiwari,Chaturvedi, Vinita,Manju,Srivastava,Giakwad,Sinha,Tripathi

, p. 4526 - 4530 (2007/10/03)

An efficient, high yield and one-pot synthesis of phenyl cyclopropyl methanones by reaction of different aryl alcohols with 4′-fluoro-4-chloro- butyrophenone in THF/DMF in the presence of NaH/TBAB is reported. Most of the methanones were further reduced t

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