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

146902-83-2

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146902-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146902-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,9,0 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 146902-83:
(8*1)+(7*4)+(6*6)+(5*9)+(4*0)+(3*2)+(2*8)+(1*3)=142
142 % 10 = 2
So 146902-83-2 is a valid CAS Registry Number.

146902-83-2Downstream Products

146902-83-2Relevant academic research and scientific papers

[Ph3C][B(C6F5)4]: A Highly Efficient Metal-Free Single-Component Initiator for the Helical-Sense-Selective Cationic Copolymerization of Chiral Aryl Isocyanides and Achiral Aryl Isocyanides

Yan, Xinwen,Zhang, Shaowen,Zhang, Pengfei,Wu, Xiaolu,Liu, An,Guo, Ge,Dong, Yuping,Li, Xiaofang

, p. 8947 - 8952 (2018)

Commercially available [Ph3C][B(C6F5)4] served as a highly efficient metal-free and single-component initiator not only for the carbocationic polymerization of polar and bulky aryl isocyanides with extremely high activity up to 1.2×107 g of polymer/(molcat. h), but also for the helical-sense-selective polymerization of chiral aryl isocyanides and copolymerization with achiral aryl isocyanides to afford high-molecular-weight functional poly(aryl isocyanide)s with good solubility as well as AIE characteristics and/or a single-handed helical conformation.

Copper-free Sandmeyer-type Reaction for the Synthesis of Sulfonyl Fluorides

Zhong, Tao,Pang, Meng-Ke,Chen, Zhi-Da,Zhang, Bin,Weng, Jiang,Lu, Gui

, p. 3072 - 3078 (2020/04/10)

A copper-free Sandmeyer-type fluorosulfonylation reaction is reported. Utilizing Na2S2O5 and Selectfluor as the sulfur dioxide and fluorine sources, respectively, aryldiazonium salts were transformed into sulfonyl fluorides. The one-pot direct synthesis of sulfonyl fluorides from aromatic amines was also realized via in situ diazotization. The practicality of this method was demonstrated by the broad functional group tolerance, gram-scale synthesis, and late-stage fluorosulfonylation of natural products and pharmaceuticals.

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