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38226-10-7

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38226-10-7 Usage

Uses

2-FLUORO-6-HYDROXYBENZALDEHYDE is used in the preparation of aromatic compounds as human PAI-1 inhibitors.

Check Digit Verification of cas no

The CAS Registry Mumber 38226-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,2 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38226-10:
(7*3)+(6*8)+(5*2)+(4*2)+(3*6)+(2*1)+(1*0)=107
107 % 10 = 7
So 38226-10-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H5FO2/c8-6-2-1-3-7(10)5(6)4-9/h1-4,10H

38226-10-7 Well-known Company Product Price

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  • Alfa Aesar

  • (L19900)  6-Fluorosalicylaldehyde, 97%   

  • 38226-10-7

  • 250mg

  • 465.0CNY

  • Detail
  • Alfa Aesar

  • (L19900)  6-Fluorosalicylaldehyde, 97%   

  • 38226-10-7

  • 1g

  • 1442.0CNY

  • Detail

38226-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Fluoro-6-hydroxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 2-FLUORO-6-HYDROXYBENZALDEHYDE

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:38226-10-7 SDS

38226-10-7Relevant articles and documents

C- ARYL GLYCOSID DERIVATIVES, PHARMACEUTICAL COMPOSITION, PREPARATION PROCESS AND USES THEREOF

-

, (2017/04/19)

This invention relates to a kind of C-aryl glycoside derivatives, its pharmaceutical compositions, preparation methods, and uses thereof. The preparation method comprises: method 1: in a solvent, deprotecting the acetyl protecting groups of compound 1-f in the presence of a base; method 2: 1) compound 2-g reacts with via Mitsunobu reaction; 2) deprotecting the acetyl protecting groups of compound 2-f obtained from step 1; method 3: 1) compound 2-g reacts with via nucleophilic substitution reaction; 2) deprotecting the acetyl protecting groups of compound 3-f obtained from step 1. The pharmaceutical composition comprises a kind of C-aryl glycoside derivatives; it's pharmaceutically acceptable salts and/or prodrugs thereof and excipient thereof. This invention further relates to a kind of C-aryl glycoside derivatives, it's pharmaceutically acceptable salts or pharmaceutical compositions thereof for the use in preparation of a SGLT inhibitor. The C-aryl glycoside derivatives of this invention provides a new direction for the study of SGLT inhibitors.

Pd-Catalyzed Ortho C-H Hydroxylation of Benzaldehydes Using a Transient Directing Group

Chen, Xiao-Yang,Ozturk, Seyma,Sorensen, Erik J.

supporting information, p. 6280 - 6283 (2017/12/08)

The direct Pd-catalyzed ortho C-H hydroxylation of benzaldehydes was achieved using 4-chloroanthranilic acid as the transient directing group, 1-fluoro-2,4,6-trimethylpyridnium triflate as the bystanding oxidant, and p-toluenesulfonic acid as the putative oxygen nucleophile. The unusual C-H chlorination and polyfluoroalkoxylation reactions signaled the importance of external nucleophiles to the outcome of Pd(IV) reductive eliminations.

PAI-1 INHIBITOR

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Page/Page column 271-272, (2011/02/17)

The compound represented by the following formula (I) and the like have PAI-1 inhibition activity; wherein: R1 represents a C6-10 aryl group which may be substituted or the like; T represents a single bond or the like; m represents 0

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