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82592-68-5

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82592-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82592-68-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,5,9 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82592-68:
(7*8)+(6*2)+(5*5)+(4*9)+(3*2)+(2*6)+(1*8)=155
155 % 10 = 5
So 82592-68-5 is a valid CAS Registry Number.

82592-68-5SDS

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-acetyloxy-4-(3-chloro-3-oxoprop-1-enyl)phenyl] acetate

1.2 Other means of identification

Product number -
Other names 2-Propenoyl chloride,3-[3,4-bis(acetyloxy)phenyl]

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:82592-68-5 SDS

82592-68-5Relevant articles and documents

Sevanol and its analogues: Chemical synthesis, biological effects and molecular docking

Belozerova, Olga A.,Osmakov, Dmitry I.,Vladimirov, Andrey,Koshelev, Sergey G.,Chugunov, Anton O.,Andreev, Yaroslav A.,Palikov, Victor A.,Palikova, Yulia A.,Shaykhutdinova, Elvira R.,Gvozd, Artem N.,Dyachenko, Igor A.,Efremov, Roman G.,Kublitski, Vadim S.,Kozlov, Sergey A.

, p. 1 - 21 (2020)

Among acid-sensing ion channels (ASICs), ASIC1a and ASIC3 subunits are the most widespread and prevalent in physiological and pathophysiological conditions. They participate in synaptic plasticity, learning and memory, as well as the perception of inflamm

Development trans-N-benzyl hydroxyl cinnamamide based compounds from cinnamic acids and characteristics anticancer potency

Agustan, Agustan,Bahriah, Bahriah,Dali, Seniwati,Firdausiah, Syadza,Rasyid, Herlina,Soekamto, Nunuk Hariani,Tahir, Dahlang,Zenta, Firdaus

, (2022/01/31)

The derivatization of three hydroxycinnamamides becomes trans-N-benzylhydroxycinnamamides, and their potential assay as anticancer agents has been carried out. N-benzyl-p-coumaramide (5a), N-benzylcaffeamide (5b), and N-benzylferulamide (5c) were obtained

Design, synthesis of Cinnamyl-paeonol derivatives with 1, 3-Dioxypropyl as link arm and screening of tyrosinase inhibition activity in vitro

Tang, Kai,Jiang, Yi,Zhang, Huawei,Huang, Wenli,Xie, Yundong,Deng, Chong,Xu, Hongbo,Song, Xiaomei,Xu, Hong

, (2020/12/13)

This study aimed to obtain tyrosinase inhibitors for treating hyperpigmentation. A series of cinnamyl ester analogues were designed and synthesized with cinnamic acid (CA) and peaonol compounds. The safety, melanin content and inhibitory effects of all ta

Cinnamate derivatives and application of cinnamate derivatives as tyrosinase inhibitors and gels

-

Paragraph 0077-0079; 0081; 0091-0094, (2020/08/02)

The invention discloses cinnamate derivatives and application of the cinnamate derivatives as tyrosinase inhibitors and gels, and the structural general formula of the cinnamate derivatives is shown in the specification, in the formula, X and Y independently represent any one of O, S and NH, wherein R1 and R2 independently represent any one of H, OH, methoxy, allyl and acetyl; R3 and R4 respectively and independently represent any one of H, OH, methoxy, tert-butyl dimethyl siloxy and carbethoxy, and R3 and R4 are not tert-butyl dimethyl silyl at the same time; and n is an integer from 2 to 5.The cinnamate derivatives disclosed by the invention have obvious inhibitory activity on the activity of mushroom tyrosinase diphenolic enzyme and the content of tyrosinase and melanin in melanoma cells of B16F10 mice, and can be used for preparing the tyrosinase inhibitors. Meanwhile, the cinnamate derivatives can form stable gels in olive oil and can be used as micromolecular gels for cosmeticsand the like.

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