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4-((((1R,2S,5R)-2-isopropyl-5-methylcyclohexyl)oxy)carbonyl)benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10210-95-4

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10210-95-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10210-95-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,1 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10210-95:
(7*1)+(6*0)+(5*2)+(4*1)+(3*0)+(2*9)+(1*5)=44
44 % 10 = 4
So 10210-95-4 is a valid CAS Registry Number.

10210-95-4Downstream Products

10210-95-4Relevant academic research and scientific papers

Electrochemical Difunctionalization of Alkenes by a Four-Component Reaction Cascade Mumm Rearrangement: Rapid Access to Functionalized Imides

Zhang, Xiaofeng,Cui, Ting,Zhao, Xin,Liu, Ping,Sun, Peipei

, p. 3465 - 3469 (2020)

An electrochemical four-component reaction cascade Mumm rearrangement was developed. It is a rare example of in situ generation of O-acyl isoamides for 1,3-(O→N) acyl transfer. Inexpensive, commercially available arylethylenes, aryl or heterocyclic acids, acetonitrile, and alcohols were used as substrates. A wide range of aryl acids and alcohols were tolerated and provided imides in satisfactory yields. Subsequent hydrolysis of imides could be utilized to synthesize valuable amides and β-amino alcohol derivatives.

Diastereoselective Synthesis of Thioglycosides via Pd-Catalyzed Allylic Rearrangement

Jiang, Xuefeng,Li, Jiagen,Wang, Ming

, p. 9053 - 9057 (2021/11/30)

Stereoselective glycosylation is challenging in carbohydrate chemistry. Herein, stereoselective thioglycosylation of glycals via palladium-catalyzed allylic rearrangement yields various substituents on α-isomer thioglycosides. Two comprehensive series of aryl and benzyl thioglycosides were obtained via a combination of thiosulfates with glycals derived from glucose, arabinose, galactose, and rhamnose. Furthermore, diosgenyl α-l-rhamnoside and isoquercitrin achieved selectivity via stereospecific [2,3]-sigma rearrangements of α-sulfoxide-rhamnoside and α-sulfoxide-glucoside, respectively.

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