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6175-45-7

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6175-45-7 Usage

Chemical Properties

clear yellow to salmon liquid

Uses

It is an effective photoinitiator for UV-curable acrylate-based coatings, adhesives and inks. used in UV-curable system. Particularly useful for photo curing clear acrylate-based formulations where non-yellowing is important. It is also recommended for pigmented inks where shelf life and color stability are essential.

Check Digit Verification of cas no

The CAS Registry Mumber 6175-45-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,7 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6175-45:
(6*6)+(5*1)+(4*7)+(3*5)+(2*4)+(1*5)=97
97 % 10 = 7
So 6175-45-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O2.C6H14O2.C4H10/c9-6-8(10)7-4-2-1-3-5-7;1-4-7-6(3)8-5-2;1-3-4-2/h1-6H;6H,4-5H2,1-3H3;3-4H2,1-2H3

6175-45-7 Well-known Company Product Price

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  • Alfa Aesar

  • (B24464)  2,2-Diethoxyacetophenone, 96%   

  • 6175-45-7

  • 25g

  • 393.0CNY

  • Detail
  • Alfa Aesar

  • (B24464)  2,2-Diethoxyacetophenone, 96%   

  • 6175-45-7

  • 100g

  • 1049.0CNY

  • Detail
  • Alfa Aesar

  • (B24464)  2,2-Diethoxyacetophenone, 96%   

  • 6175-45-7

  • 500g

  • 2294.0CNY

  • Detail

6175-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-Diethoxyacetophenone

1.2 Other means of identification

Product number -
Other names DEAP

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:6175-45-7 SDS

6175-45-7Relevant articles and documents

Modular Synthesis of α-Substituted Alkenyl Acetals by a Palladium-Catalyzed Suzuki Reaction of α-Haloalkenyl Acetals with Organoboranes

Zhang, Li

, p. 723 - 727 (2021/02/26)

A modular and straightforward synthetic strategy for the preparation of α-substituted alkenyl acetals has been developed. α-Haloalkenyl acetals react smoothly with (het)aryl boronic acids, aryl boronates, or B-Alkyl-9-borabicyclo[3.3.1]nonanes through Pd-catalyzed Suzuki cross-coupling under mild conditions with good to high yields. This protocol features a broad substrate scope and good functional-group compatibility, and is easily scaled up.

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.

Stereoselective Ketone Rearrangements with Hypervalent Iodine Reagents

Malmedy, Florence,Wirth, Thomas

supporting information, p. 16072 - 16077 (2016/10/30)

The first stereoselective version of an iodine(III)-mediated rearrangement of arylketones in the presence of orthoesters is described. The reaction products, α-arylated esters, are very useful intermediates in the synthesis of bioactive compounds such as ibuprofen. With chiral lactic acid-based iodine(III) reagents product selectivities of up to 73 % ee have been achieved.

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