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20274-69-5

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20274-69-5 Usage

Description

4-Fluoro-3-nitrobenzyl alcohol, also known as 4-FLUORO-3-NITROBENZYL ALCOHOL 96, is an organic compound derived from the reaction between borane and 4-fluoro-3-nitrobenzoic acid. It is a versatile chemical intermediate with potential applications in various industries due to its unique chemical properties.

Uses

Used in Pharmaceutical Industry:
4-Fluoro-3-nitrobenzyl alcohol is used as a reagent for the preparation of EW-7197 (E950000), a highly potent orally bioavailable inhibitor of TGF-β type I receptor kinase. 4-FLUORO-3-NITROBENZYL ALCOHOL 96 is utilized in cancer treatment as an immunotherapeutic or antifibrotic agent, playing a crucial role in modulating the immune response and reducing fibrosis associated with cancer progression.
Used in Chemical Synthesis:
4-Fluoro-3-nitrobenzyl alcohol may be used in the synthesis of 4-fluoro-3-nitrobenzyl chloride, which is another important chemical intermediate with potential applications in various chemical and pharmaceutical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 20274-69-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,7 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20274-69:
(7*2)+(6*0)+(5*2)+(4*7)+(3*4)+(2*6)+(1*9)=85
85 % 10 = 5
So 20274-69-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H6FNO3/c8-6-2-1-5(4-10)3-7(6)9(11)12/h1-3,10H,4H2

20274-69-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-fluoro-3-nitrophenyl)methanol

1.2 Other means of identification

Product number -
Other names 4-Fluoro-3-nitrobenzylalcohol

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:20274-69-5 SDS

20274-69-5Relevant articles and documents

TYK2 INHIBITORS AND USES THEREOF

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Paragraph 00639, (2020/09/27)

Described herein are compounds that are useful in treating a TYK2-mediated disorder. In some embodiments, the TYK2-mediated disorder is an autoimmune disorder, an inflammatory disorder, a proliferative disorder, an endocrine disorder, a neurological disorder, or a disorder associated with transplantation.

Asymmetric Total Synthesis and Evaluation of Antitumor Activity of Ophiorrhisine A and Its Derivatives

Onozawa, Tadayoshi,Kitajima, Mariko,Kogure, Noriyuki,Takayama, Hiromitsu

, p. 15312 - 15322 (2019/01/03)

The first asymmetric total synthesis of ophiorrhisine A (1), a new cyclic tetrapeptide isolated from Ophiorrhiza nutans, was accomplished via an intramolecular aromatic nucleophilic substitution reaction (IMSNAr) of a linear tripeptide to construct a 14-membered paracyclophane ring, resulting in confirmation of its structure and absolute configuration. The structure-activity relationship study of 1 and its derivatives demonstrated that some derivatives possessed cytotoxicity toward human cancer cell lines A549, HT29, and HCT116.

IMINOTETRAHYDROPYRIMIDINONE DERIVATIVES AS PLASMEPSIN V INHIBITORS

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Page/Page column 54, (2017/07/05)

A series of 2-imino-6-methyltetrahydropyrimidin-4(lH)-one derivatives, substituted in the 6-position by a phenyl moiety which in turn is meta-substituted by an optionally substituted unsaturated fused bicyclic ring system containing at least one nitrogen atom, being selective inhibitors of plasmepsin V activity, are beneficial as pharmaceutical agents, especially in the treatment of malaria.

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