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Benzene, 1-iodo-2-[(2-propen-1-yloxy)methyl]-4-(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

920334-57-2

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920334-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 920334-57-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,0,3,3 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 920334-57:
(8*9)+(7*2)+(6*0)+(5*3)+(4*3)+(3*4)+(2*5)+(1*7)=142
142 % 10 = 2
So 920334-57-2 is a valid CAS Registry Number.

920334-57-2Downstream Products

920334-57-2Relevant academic research and scientific papers

Synthesis of functionalized 3-isochromanones: Via metal-free intramolecular alkoxylation-initiated cascade cyclization

Zhang, Ying-Qi,Zhu, Xin-Qi,Xu, Yin,Bu, Hao-Zhen,Wang, Jia-Le,Zhai, Tong-Yi,Zhou, Jin-Mei,Ye, Long-Wu

supporting information, p. 3023 - 3028 (2019/06/18)

A metal-free intramolecular alkoxylation-initiated cascade cyclization of allyl ether-tethered ynamides has been developed. Various highly functionalized 3-isochromanones can be obtained in generally good to excellent yields under mild reaction conditions

Concise stereoselective synthesis of oxaspirocycles with 1-tosyl-1,2,3-triazoles: Application to the total syntheses of (±)-tuberostemospiroline and (±)-stemona-lactamr

Fu, Junkai,Shen, Hongjuan,Chang, Yuanyuan,Li, Chuangchuang,Gong, Jianxian,Yang, Zhen

supporting information, p. 12881 - 12888 (2015/03/30)

A 4-substituted-1-tosyl-1,2,3-triazole-based stereoselective synthesis of structurally diverse oxaspirocycles is reported. The synthesis involves Rh-catalyzed loss of nitrogen from 4-substituted-1-tosyl-1,2,3-triazoles, Grignard reaction, and a ring-closing metathesis reaction as key steps. By employing readily available and stable 4-substituted-1-tosyl-1,2,3-triazoles as surrogates of diazo compounds and nitrogen sources, two types of oxaspirocycles were obtained. The latter compounds, which contain adjacent nitrogen stereocenters, could serve as the core structures of many natural products. This chemistry has been successfully applied to the total syntheses of (±)-tuberostemospiroline and (±)-stemona-lactamR.

NOVEL HETEROCYCLIDENE ACETAMIDE DERIVATIVE

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Page/Page column 108, (2010/11/30)

A compound represented by formula (I'): (wherein m, n, and p each represent 0 to 2; q represents 0 or 1; R1 represents halogen, a hydrocarbon group, a heterocyclic group, an alkoxy group, an alkoxycarbonyl group, a sulfamoyl group, a CN group,

Novel Heterocyclidene Acetamide Derivative

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Page/Page column 71, (2008/12/09)

A compound represented by formula (I′): (wherein m, n, and p each represent 0 to 2; q represents 0 or 1; R1 represents halogen, a hydrocarbon group, a heterocyclic group, an alkoxy group, an alkoxycarbonyl group, a sulfamoyl group, a CN group,

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