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93651-42-4

cis-(γ-Phenyl-allyl)-(3.5-dimethyl-phenyl)-ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93651-42-4 Structure

  • Basic information

    1. Product Name: cis-(γ-Phenyl-allyl)-(3.5-dimethyl-phenyl)-ether
    2. Synonyms: cis-(γ-Phenyl-allyl)-(3.5-dimethyl-phenyl)-ether
    3. CAS NO:93651-42-4
    4. Molecular Formula:
    5. Molecular Weight: 238.329
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93651-42-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: cis-(γ-Phenyl-allyl)-(3.5-dimethyl-phenyl)-ether(CAS DataBase Reference)
    10. NIST Chemistry Reference: cis-(γ-Phenyl-allyl)-(3.5-dimethyl-phenyl)-ether(93651-42-4)
    11. EPA Substance Registry System: cis-(γ-Phenyl-allyl)-(3.5-dimethyl-phenyl)-ether(93651-42-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 93651-42-4(Hazardous Substances Data)

93651-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93651-42-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,6,5 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93651-42:
(7*9)+(6*3)+(5*6)+(4*5)+(3*1)+(2*4)+(1*2)=144
144 % 10 = 4
So 93651-42-4 is a valid CAS Registry Number.

93651-42-4Relevant articles and documents

Palladium-Catalyzed Aerobic Oxygenation of Allylarenes

Li, Chunsheng,Li, Meng,Li, Jianxiao,Liao, Jianhua,Wu, Wanqing,Jiang, Huanfeng

, p. 10912 - 10919 (2017/10/27)

An efficient and practical protocol for the synthesis of (E)-allylethers from readily available olefins with alcohols or phenols was developed. This aerobic oxidative allylic C-H oxygenation protocol features mild conditions, broad substrate scope, and hi

From precursor to catalyst: The involvement of [Ru(η5-Cp?)Cl2]2 in highly branch selective allylic etherification of cinnamyl chlorides

Siddappa, Ravi Kumara Guralamatta,Chang, Chih-Wei,Chein, Rong-Jie

supporting information, p. 1031 - 1035 (2015/02/19)

(RuCp?Cl2)2, a general entry into Cp?Ru sandwich and half-sandwich chemistry was first used as a precatalyst in allylic etherification of cinnamyl chlorides with up to 98:2 regioselectivity (19 examples). Both the solvent effect and the exsiccant reaction condition are crucial to the reactivity and selectivity. Preliminary mechanism studies and the demonstration of Fluoxetine synthesis were presented in this work as well.

Synthesis and structure of [Ru(PPh3)2(bipy)(MeCN)Cl][BPh4] and it's catalytic property towards regioselective and stereoselective allylation of phenols

Sinha, Abhilasha,Khatua, Snehadrinarayan,Bhattacharjee, Manish

supporting information, p. 116 - 120 (2015/02/19)

The compound, [Ru(PPh3)2(bipy)(MeCN)Cl][BPh4] (1) has been synthesized from the precursor complex, [Ru(bipy)(PPh3)2Cl2]. The complex has been structurally characterized. This complex has been found to be an efficient catalyst for the regioselective allylation of phenols.

From precursor to catalyst: The involvement of [Ru(η5- Cp*)Cl2]2 in highly branch selective allylic etherification of cinnamyl chlorides

Siddappa, Ravi Kumara Guralamatta,Chang, Chih-Wei,Chein, Rong-Jie

supporting information, p. 1031 - 1035 (2014/02/14)

(RuCp*Cl2)2, a general entry into Cp*Ru sandwich and half-sandwich chemistry was first used as a precatalyst in allylic etherification of cinnamyl chlorides with up to 98:2 regioselectivity (19 examples). Both the solvent effect and the exsiccant reaction condition are crucial to the reactivity and selectivity. Preliminary mechanism studies and the demonstration of Fluoxetine synthesis were presented in this work as well.

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