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1-(3-((t-butyldimethylsilyl)oxy)prop-1-yn-1-yl)cyclohexyl methyl carbonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1360733-83-0

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1360733-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1360733-83-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,7,3 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1360733-83:
(9*1)+(8*3)+(7*6)+(6*0)+(5*7)+(4*3)+(3*3)+(2*8)+(1*3)=150
150 % 10 = 0
So 1360733-83-0 is a valid CAS Registry Number.

1360733-83-0Relevant academic research and scientific papers

Synthesis of Functionalized [3], [4], [5] and [6]Dendralenes through Palladium-Catalyzed Cross-Couplings of Substituted Allenoates

Lippincott, Daniel J.,Linstadt, Roscoe T. H.,Maser, Michael R.,Lipshutz, Bruce H.

supporting information, p. 847 - 850 (2017/01/14)

A mild method for the synthesis of highly functionalized [3]–[6]dendralenes is reported, representing a general strategy to diversely substituted higher homologues of the dendralenes. The methodology utilizes allenoates bearing various substitution patter

α-fluoroallenoate synthesis via N-heterocyclic carbene-catalyzed fluorination reaction of alkynals

Wang, Xu,Wu, Zijun,Wang, Jian

supporting information, p. 576 - 579 (2016/02/18)

The first catalytic α-fluoroallenoate synthesis is described. With a suitable combination of N-heterocyclic carbene precatalyst, base, and fluorine reagent, the reaction proceeded smoothly to yield a wide range of α-fluoroallenoates with excellent chemose

N -heterocyclic carbene-catalyzed internal redox reaction of alkynals: An efficient synthesis of allenoates

Zhao, Yu-Ming,Tam, Yik,Wang, Yu-Jie,Li, Zigang,Sun, Jianwei

supporting information; experimental part, p. 1398 - 1401 (2012/06/01)

An efficient N-heterocyclic carbene (NHC)-catalyzed internal redox reaction of alkynals that bear a γ leaving group has been developed. This process provides a new access to a range of allenoates in good yields. Preliminary results demonstrate that the en

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