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3-benzyl-2-hydroxybenzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

131628-72-3

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131628-72-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131628-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,6,2 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 131628-72:
(8*1)+(7*3)+(6*1)+(5*6)+(4*2)+(3*8)+(2*7)+(1*2)=113
113 % 10 = 3
So 131628-72-3 is a valid CAS Registry Number.

131628-72-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzylsalicylaldehyde

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:131628-72-3 SDS

131628-72-3Downstream Products

131628-72-3Relevant academic research and scientific papers

Cobalt-Nitrenoid Insertion-Mediated Amidative Carbon Rearrangement via Alkyl-Walking on Arenes

Lee, Jeonghyo,Kang, Bora,Kim, Dongwook,Lee, Jia,Chang, Sukbok

supporting information, p. 18406 - 18412 (2021/11/16)

We herein disclose the Cp*Co(III)(LX)-catalyzed amidative alkyl migration using 2,6-disubstituted phenyl azidoformates. Upon the cobalt-nitrenoid insertion toward the substituted ortho carbon, an arenium cationic species bearing a quaternary carbon is generated, and a subsequent alkyl migration process is suggested to occur through an unforeseen alkyl-walking mechanism. A quinolinol ligand of the cobalt catalyst system is proposed to facilitate the final product-releasing rearomatization process by serving as an internal base. This new mechanistic mode enabled both [1,2]- and [1,4]-alkyl rearrangements to allow the structural variation of N-heterocyclic compounds.

Acidic rearrangement of (benzyloxy)chalcones: A short synthesis of chamanetin

Sagrera, Gabriel,Seoane, Gustavo

scheme or table, p. 4190 - 4202 (2011/03/20)

Treatment of (benzyloxy)chalcones with trifluoroacetic acid in refluxing chloroform gave several new benzyl(hydroxy)flavanones in high yields and good regioselectivities. By using this procedure, we prepared the natural compound chamanetin in good yield from readily available reagents. Georg Thieme Verlag Stuttgart - New York.

Solid-supported acids for debenzylation of aryl benzyl ethers

Petchmanee, Thaninee,Ploypradith, Poonsakdi,Ruchirawat, Somsak

, p. 2892 - 2895 (2007/10/03)

Solid-supported acids have been investigated for aromatic debenzylation reactions. Stoichiometric amounts of solid-supported acids in refluxing toluene with or without 4 equiv of methanol effectively provided the desired aromatic debenzylation products of various systems in moderate to excellent yields (up to 98%).

SUBSTITUTED INDOLE, BENZOFURAN AND BENZOTHIOPHENE DERIVATIVES AS 5-LIPOXYGENASE INHIBITORS

-

, (2008/06/13)

Provided are substituted indoles, benzofurans, and benzothiophenes of the formula wherein X, R2 and R3 are described in the specification. These compounds are 5-lipoxygenase inhibitors and are useful as antiinflammatory agents.

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