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5-[(1E)-2-(4-Chlorophenyl)ethenyl]-1,3-benzenediol, also known as 4'-chloro-5-stilbenol, is a chemical compound with a molecular formula C14H11ClO2. It is a derivative of stilbene and belongs to the class of dihydroxybenzenes. 5-[(1E)-2-(4-Chlorophenyl)ethenyl]-1,3-benzenediol is a white to off-white crystalline powder that is insoluble in water but soluble in organic solvents.

823804-63-3

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823804-63-3 Usage

Uses

Used in Pharmaceutical Industry:
5-[(1E)-2-(4-Chlorophenyl)ethenyl]-1,3-benzenediol is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into complex organic compounds, contributing to the development of new medications.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, 5-[(1E)-2-(4-Chlorophenyl)ethenyl]-1,3-benzenediol serves as a key intermediate, facilitating the creation of a variety of organic compounds for research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 823804-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,3,8,0 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 823804-63:
(8*8)+(7*2)+(6*3)+(5*8)+(4*0)+(3*4)+(2*6)+(1*3)=163
163 % 10 = 3
So 823804-63-3 is a valid CAS Registry Number.

823804-63-3SDS

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 5-[2-(4-chlorophenyl)ethenyl]benzene-1,3-diol

1.2 Other means of identification

Product number -
Other names -

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:823804-63-3 SDS

823804-63-3Downstream Products

823804-63-3Relevant academic research and scientific papers

Resveratrol derivative and application thereof

-

Paragraph 0049-0052, (2020/12/30)

The invention provides a resveratrol derivative shown as a formula (II), in the formula (II), when R1 is hydroxyl, halogen, C1-C4 alkyl or C1-C4 methoxy, R2 is H; when R1 is H, R2 is halogen; and particularly, when R1 is hydroxyl, halogen, C1-C4 alkyl or C1-C4 methoxy, R2 is H preferably. According to the new compound resveratrol derivative and the preparation method thereof, the operation processis simple, raw material sources are commercialized and easy to obtain, and compared with resveratrol and 7-hydroxy coumarin, the inhibition effect is remarkably improved. Compared with the previous resveratrol modification method, the method has the advantages that the reaction is completed in one step, and is more direct, efficient and rapid.

Synthesis of resveratrol derivatives as new analgesic drugs through desensitization of the TRPA1 receptor

Nakao, Syuhei,Mabuchi, Miyuki,Wang, Shenglan,Kogure, Yoko,Shimizu, Tadashi,Noguchi, Koichi,Tanaka, Akito,Dai, Yi

supporting information, p. 3167 - 3172 (2017/06/13)

A series of 31 resveratrol derivatives was designed, synthesized and evaluated for activation and inhibition of the TRPA1 channel. Most acted as activators and desensitizers of TRPA1 channels like resveratrol or allyl isothiocyanate (AITC). Compound 4z (HUHS029) exhibited higher inhibitory activity than resveratrol with an IC50 value of 16.1?μM. The activity of 4z on TRPA1 was confirmed in TRPA1-expressing HEK293 cells, as well as in rat dorsal root ganglia neurons by a whole cell patch clamp recording. Furthermore, pretreatment with 4z exhibited an analgesic effect on AITC-evoked TRPA1-related pain behavior in vivo.

A facile and rapid access to resveratrol derivatives and their radioprotective activity

Uzura, Saori,Sekine-Suzuki, Emiko,Nakanishi, Ikuo,Sonoda, Motohiro,Tanimori, Shinji

, p. 3886 - 3891 (2016/08/01)

A facile and rapid access to resveratrol derivatives has been achieved based on palladium-catalyzed oxidative Heck reaction of aryl boronic acids with styrenes followed by demethylation in moderate to good yields. A series of resveratrol derivatives with various functional groups has been synthesized easily. The radioprotective activity of synthesized compounds has also been evaluated using rat thymocytes. The results revealed that some resveratrol derivatives efficiently protected the thymocytes from radiation-induced apoptosis.

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