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1046161-84-5

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1046161-84-5 Usage

General Description

2-Propenal, 3-(2-chlorophenyl)-2-Methyl- is a chemical compound with the molecular formula C10H8Cl2O. It is also known by its common name, chlorobenzaldehyde. 2-Propenal, 3-(2-chlorophenyl)-2-Methyl- is a yellow liquid with a pungent, almond-like odor. It is used as an intermediate in the production of various chemicals and pharmaceuticals, and also as a flavoring agent in food products. The compound is toxic and may cause irritation to the skin, eyes, and respiratory system, and should be handled with care. Additionally, it is important to follow proper safety precautions when working with this chemical to minimize the risk of exposure and potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 1046161-84-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,6,1,6 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1046161-84:
(9*1)+(8*0)+(7*4)+(6*6)+(5*1)+(4*6)+(3*1)+(2*8)+(1*4)=125
125 % 10 = 5
So 1046161-84-5 is a valid CAS Registry Number.

1046161-84-5Downstream Products

1046161-84-5Relevant articles and documents

Tetraalkylammonium and 1,3-dialkylimidazolium salts with fluorinated anions as recoverable phase-transfer catalysts in solid base-promoted cross-aldol condensations

Kryshtal, Galina V.,Zhdankina, Galina M.,Zlotin, Sergei G.

, p. 2822 - 2827 (2005)

Tetraalkylammonium and 1,3-dialkylimidazolium tetrafluoroborates and hexafluorophosphates were employed for the first time as recoverable phase-transfer catalysts in multiphase reactions of CH-acids, in particular in solid base-pro-moted cross-aldol condensations. The catalysts retained their catalytic activity over several reaction cycles.

Copper-Catalyzed Stereospecific Hydroboration of Internal Allylic Alcohols

Ji, Enhui,Meng, Haiwen,Zheng, Yue,Ramadoss, Velayudham,Wang, Yahui

supporting information, p. 7367 - 7371 (2019/11/22)

An effective Cu-catalyzed stereospecific hydroboration of aliphatic and aromatic 1,1,2-trisubstituted internal allylic alcohols has been reported. This reaction proceeds via a silyl ether transient protection of allylic alcohols and subsequent stereospecific hydroboration. Followed by an oxidative workup, an array of acyclic, cyclic, and heterocyclic 1,3-diols was synthesized in good to excellent yields with good functional group tolerance and excellent diastereomeric ratios (> 20:1).

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