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71648-21-0

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71648-21-0 Usage

Description

3-Ethoxybenzyl alcohol is an organic compound derived from m-anisaldehyde through a reduction process in the presence of lithium aluminum hydride (LiAlH4) and ether. It is characterized by the presence of an ethoxy group attached to a benzene ring with a hydroxyl group, which gives it unique chemical properties and potential applications in various industries.

Uses

Used in Pharmaceutical Industry:
3-Ethoxybenzyl alcohol is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a versatile building block for the development of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
In the field of organic chemistry, 3-ethoxybenzyl alcohol serves as a valuable intermediate for the synthesis of a wide range of organic compounds. Its reactivity and functional groups make it suitable for various chemical reactions, leading to the formation of new molecules with diverse properties and applications.
Used in Flavor and Fragrance Industry:
Due to its aromatic nature, 3-ethoxybenzyl alcohol can be used as a component in the flavor and fragrance industry. Its pleasant odor and ability to blend well with other compounds make it a potential candidate for creating unique scents and flavors in various consumer products.
Used in Material Science:
3-Ethoxybenzyl alcohol can be utilized in the development of new materials with specific properties. Its chemical structure can be incorporated into polymers, coatings, or other materials to impart desired characteristics such as improved stability, enhanced reactivity, or specific interactions with other molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 71648-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,4 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71648-21:
(7*7)+(6*1)+(5*6)+(4*4)+(3*8)+(2*2)+(1*1)=130
130 % 10 = 0
So 71648-21-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O2/c1-2-11-9-5-3-4-8(6-9)7-10/h3-6,10H,2,7H2,1H3

71648-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-ethoxyphenyl)methanol

1.2 Other means of identification

Product number -
Other names (3-ethoxyphenyl)methan-1-ol

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:71648-21-0 SDS

71648-21-0Relevant articles and documents

Discovery and optimization of novel N-benzyl-3,6-dimethylbenzo[d]isoxazol-5-amine derivatives as potent and selective TRIM24 bromodomain inhibitors with potential anti-cancer activities

Hu, Qingqing,Wang, Chao,Xiang, Qiuping,Wang, Rui,Zhang, Cheng,Zhang, Maofeng,Xue, Xiaoqian,Luo, Guolong,Liu, Xiaomin,Wu, Xishan,Zhang, Yan,Wu, Donghai,Xu, Yong

, (2019/12/26)

Tripartite motif-containing protein 24 (TRIM24), recognized as an epigenetic reader for acetylated H3K23 (H3K23ac) via its bromodomain, has been closely involved in tumorigenesis or tumor progression of several cancers. Developing inhibitors of TRIM24 is significant for functional studies and drug discovery. Herein, we report the identification, optimization and evaluation of N-benzyl-3,6-dimethylbenzo[d]isoxazol-5-amines as TRIM24 bromodomain inhibitors starting from an in house library screening. Structure-based optimization leads to two potent and selective compounds 11d and 11h in an Alphascreen assay with IC50 values of 1.88 μM and 2.53 μM, respectively. The viability assay demonstrates the great potential of this series of compounds as inhibitors of proliferation of prostate cancer (PC) cells LNCaP, C4-2B. A colony formation assay further supports this inhibitory activity. Compounds 11d and 11h inhibit cell proliferation of other cancer types such as non-small cell lung cancer (NSCLC) cells A549 with IC50 values of 1.08 μM and 0.75 μM, respectively. These data suggests that compounds 11d and 11h are promising lead compounds for further research.

Cyclic compounds and uses thereof

-

, (2008/06/13)

Compounds of general formula (1) R1—X1—W—X2—Z1—Z2—R2 or salts thereof, exhibiting preventive and therapeutic effects against HIV infectious diseases wherein R1is an optionally substituted five- or six-membered ring group; X1is a free valency or the like; W is a divalent group represented by, e. g., general formula (2) (wherein A and B are each an optionally substituted five- to seven-membered ring; E1and E4are each optionally substituted carbon or the like; E2and E3are each oxygen or the like; and a and b are each a single bond or a double bond); X2is a divalent group constituting a straight chain moiety; Z1is a divalent cyclic group or the like; Z2is a free valency or the like; and R2is optionally substituted amino or the like.

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