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Ethanone, 1-[2,6-bis(acetyloxy)phenyl]-, also known as a benzophenone derivative, is an organic chemical compound characterized by its ability to absorb and filter ultraviolet (UV) light. It features a phenyl ring with two acetyloxy groups attached, which contribute to its enhanced UV protection capabilities. Ethanone, 1-[2,6-bis(acetyloxy)phenyl]is a valuable ingredient in cosmetic and skincare formulations due to its photoprotective properties.

144152-28-3

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144152-28-3 Usage

Uses

Used in Cosmetics and Skincare Industry:
Ethanone, 1-[2,6-bis(acetyloxy)phenyl]is used as a UV filter in sunscreens for its ability to absorb and filter ultraviolet light, providing photoprotection to the skin and preventing sunburn and skin damage caused by UV radiation.
Used in Hair Care Products:
In the hair care industry, Ethanone, 1-[2,6-bis(acetyloxy)phenyl]is used as a UV protectant in hair care products to shield hair from the damaging effects of UV light, which can lead to hair dryness, brittleness, and color fading. Its inclusion in hair care formulations helps maintain hair health and appearance.

Check Digit Verification of cas no

The CAS Registry Mumber 144152-28-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,1,5 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 144152-28:
(8*1)+(7*4)+(6*4)+(5*1)+(4*5)+(3*2)+(2*2)+(1*8)=103
103 % 10 = 3
So 144152-28-3 is a valid CAS Registry Number.

144152-28-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-acetyl-3-acetyloxyphenyl) acetate

1.2 Other means of identification

Product number -
Other names 2,6-Diacetoxyacetophenon

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:144152-28-3 SDS

144152-28-3Relevant academic research and scientific papers

Synthesis of substituted 2,3-dihydrobenzofuran in a process involving a facile acyl migration

Li, Wen-Sen,Guo, Zhenrong,Thornton, John,Katipally, Kishta,Polniaszek, Richard,Thottathil, John,Vu, Truc,Wong, Michael

, p. 1923 - 1925 (2002)

Reduction of 2,6-diacetoxy-2′-bromoacetophenone (10) with NaBH4 led to 3,4-diacetoxydihydrobenzofuran (12) in a process involving acyl migration followed by cyclization. Subsequent hydrogenolysis gave 4-acetoxydihydrobenzofuran which, upon saponification, afforded 4-hydroxydihydrobenzofuran (8) in good yield. This approach is shown to be a general method for preparation of substituted dihydrobenzofurans.

A method of cosmetic depigmentation care by applying at least one aurone

-

Page/Page column 13, (2008/06/13)

At least one aurone or a natural or synthetic derivative of aurone, or an analogue of aurone, in which the independent phenyl ring can be substituted by a heterocycle of pyrrole, imidazole, triazole, pyridine, furan, or thiophene type, is disclosed as a cosmetic agent, or as an active substance, for the manufacture either of a cosmetic composition, or of a pharmaceutical composition, notably a dermatological composition, having a melanogenesis-inhibiting activity or a depigmenting activity, or an anti-tyrosinase activity.

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