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Ethanone, 1-phenyl-2,2-dipropoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54149-75-6

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54149-75-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54149-75-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,4 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54149-75:
(7*5)+(6*4)+(5*1)+(4*4)+(3*9)+(2*7)+(1*5)=126
126 % 10 = 6
So 54149-75-6 is a valid CAS Registry Number.

54149-75-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-2,2-dipropoxyethanone

1.2 Other means of identification

Product number -
Other names 2,2-dipropoxyacetophenone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:54149-75-6 SDS

54149-75-6Downstream Products

54149-75-6Relevant academic research and scientific papers

Synergistic Catalysis of Se and Cu for the Activation of α-H of Methyl Ketones with Molecular Oxygen/Alcohol to Produce α-Keto Acetals?

Chen, Chao,Cao, Zhicheng,Zhang, Xu,Li, Yiming,Yu, Lei,Jiang, Xuefeng

, p. 1045 - 1051 (2020/06/30)

Selenium and copper synergistically catalyzed the oxidation/alkoxylation of methyl ketones to synthesize α-keto acetals directly. Using O2 as oxidant and alcohol as solvent and alkoxylation reagent, the reaction is practical from industrial viewpoint. Mechanistic studies revealed that copper promoted the oxidation of organoselenium intermediates with O2 to allow the key rearrangement and selenoxide syn-elimination regenerating the catalytically active organoselenium species.

LIQUID-PHASE DIALKOXYLATION OF ACETOPHENONE

Gordeeva, G. N.,Kalashnikov, S. M.,Popov, Yu. N.,Kruglov, E. A.,Imashev, U. B.

, p. 1975 - 1978 (2007/10/02)

The treatment of acetophenone with alkyl nitrites in the presence of the corresponding aliphatic alcohols and hydrochloric acid leads to the formation of phenylglyoxal acetals.The structures of the products were established by IR, UV, NMR, and mass spectroscopy.

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