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Benzene, 1-(cyclohexyloxy)-4-(1,1-dimethylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31582-86-2

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31582-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31582-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,5,8 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31582-86:
(7*3)+(6*1)+(5*5)+(4*8)+(3*2)+(2*8)+(1*6)=112
112 % 10 = 2
So 31582-86-2 is a valid CAS Registry Number.

31582-86-2Downstream Products

31582-86-2Relevant academic research and scientific papers

Gold(I)-catalyzed intermolecular addition of phenols and carboxylic acids to olefins

Yang, Cai-Guang,He, Chuan

, p. 6966 - 6967 (2005)

Ph3PAuOTf can catalyze efficient intermolecular addition of phenols and carboxylic acids to olefins under relatively mild conditions. Copyright

Chemoselective, Scalable Nickel-Electrocatalytic O-Arylation of Alcohols

Baran, Phil S.,Chen, Longrui,Edwards, Jacob T.,Kawamata, Yu,Oderinde, Martins S.,Zhang, Hai-Jun

supporting information, p. 20700 - 20705 (2021/08/17)

The formation of aryl-alkyl ether bonds through cross coupling of alcohols with aryl halides represents a useful strategic departure from classical SN2 methods. Numerous tactics relying on Pd-, Cu-, and Ni-based catalytic systems have emerged over the past several years. Herein we disclose a Ni-catalyzed electrochemically driven protocol to achieve this useful transformation with a broad substrate scope in an operationally simple way. This electrochemical method does not require strong base, exogenous expensive transition metal catalysts (e.g., Ir, Ru), and can easily be scaled up in either a batch or flow setting. Interestingly, e-etherification exhibits an enhanced substrate scope over the mechanistically related photochemical variant as it tolerates tertiary amine functional groups in the alcohol nucleophile.

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