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74047-22-6

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74047-22-6 Usage

General Description

2-Ethynyl-4-hydroxy-phenol is a chemical compound that belongs to the family of phenols. It is a derivative of phenol with an ethynyl group attached to the carbon at position 2. 2-ETHYNYL-4-HYDROXY-PHENOL is a pale yellow solid at room temperature and is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. It is also used as a building block in the production of polymers and other industrial materials. Additionally, 2-ethynyl-4-hydroxy-phenol has been studied for its potential antioxidant and anti-inflammatory properties, making it a subject of interest in the field of medicinal and pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 74047-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,0,4 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74047-22:
(7*7)+(6*4)+(5*0)+(4*4)+(3*7)+(2*2)+(1*2)=116
116 % 10 = 6
So 74047-22-6 is a valid CAS Registry Number.

74047-22-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethynylbenzene-1,4-diol

1.2 Other means of identification

Product number -
Other names 2-ETHYNYL-4-HYDROXY-PHENOL

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:74047-22-6 SDS

74047-22-6Relevant articles and documents

A rapid synthesis of lavendustin-mimetic small molecules by click fragment assembly

Yoon, Jieun,Ryu, Jae-Sang

supporting information; experimental part, p. 3930 - 3935 (2010/08/20)

Lavendustin-mimetic small molecules modifying the linker -CH 2-NH- with an 1,2,3-triazole ring have been synthesized via a click chemistry. Two pharmacophoric fragments of lavendustin were varied to investigate chemical space and the auxophoric -CH2-NH- was altered to an 1,2,3-triazole for rapid click conjugation. The small molecules were evaluated against HCT116 colon cancer and CCRF-CEM leukemia cell lines. Among 28 analogues, 3-phenylpropyl ester 26b inhibited CCRF-CEM leukemia cell growth with GI50 value of 0.9 μM.

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