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4-Hydroxy-2-isopropoxybenzaldehyde is an organic compound with the chemical formula C10H12O3. It is a derivative of benzaldehyde, featuring a hydroxyl group at the 4-position and an isopropoxy group at the 2-position. This aldehyde is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique functional groups. The presence of the hydroxyl and isopropoxy groups allows for further chemical reactions, making it a valuable intermediate in organic synthesis. The compound is characterized by its ability to form Schiff bases and other condensation products, which are important in the preparation of complex organic molecules.

1165713-47-2

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1165713-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1165713-47-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,5,7,1 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1165713-47:
(9*1)+(8*1)+(7*6)+(6*5)+(5*7)+(4*1)+(3*3)+(2*4)+(1*7)=152
152 % 10 = 2
So 1165713-47-2 is a valid CAS Registry Number.

1165713-47-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-2-isopropoxybenzaldehyde

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

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More Details:1165713-47-2 SDS

1165713-47-2Downstream Products

1165713-47-2Relevant academic research and scientific papers

PRODRUGS OF OXAZOLIDINONE CETP INHIBITORS

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Page/Page column 19, (2010/04/27)

The compounds of Formula I are prodrugs of CETP inhibitors having a central oxazolidinone ring. The compounds cyclize by the elimination of HX to form an oxazolidinone ring after administration to a patient.

Factors affecting orthogonality in the deprotection of 2,4-di-protected aromatic ethers employing solid-supported acids

Tangdenpaisal, Kassrin,Sualek, Supannee,Ruchirawat, Somsak,Ploypradith, Poonsakdi

experimental part, p. 4316 - 4325 (2009/10/17)

Selective deprotection of aromatic ethers bearing two protecting groups on the same aromatic ring by solid-supported acids (Amberlyst-15 and PTS-Si) was systematically investigated. ortho-Directing protonation by the carbonyl group as well as carbocation stability and quenching are the important determining factors for the orthogonal deprotection process. Stablilized carbocations (e.g., those from the MOM and PMB groups) could be removed with high selectivity.

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