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Antiarolaldehyde, also known as 2,3,4,5-tetrahydro-3,5-dihydroxy-6-methyl-1-(2H)-pyridinecarboxaldehyde, is a naturally occurring chemical compound found in the bark of the Antiaris toxicaria tree. It is a colorless solid with a molecular formula of C7H9NO3 and a molecular weight of 157.15 g/mol. Antiarolaldehyde has been studied for its potential anti-inflammatory, analgesic, and antipyretic properties, as well as its ability to inhibit the release of histamine and prostaglandins. It is also known for its cytotoxic effects on certain cancer cell lines, making it a subject of interest in the field of natural product chemistry and drug discovery.

832-65-5

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832-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 832-65-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 832-65:
(5*8)+(4*3)+(3*2)+(2*6)+(1*5)=75
75 % 10 = 5
So 832-65-5 is a valid CAS Registry Number.

832-65-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-4,5,6-trimethoxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 4,5,6-trimethoxysalicylaldehyde

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:832-65-5 SDS

832-65-5Relevant academic research and scientific papers

Formylation of electron-rich aromatic rings mediated by dichloromethyl methyl ether and TiCl4: Scope and limitations

Ramos-Tomillero, Iván,Paradís-Bas, Marta,De Pinho Ribeiro Moreira, Ibério,Bofill, Josep María,Nicolás, Ernesto,Albericio, Fernando

supporting information, p. 5409 - 5422 (2015/05/13)

Here the aromatic formylation mediated by TiCl4 and dichloromethyl methyl ether previously described by our group has been explored for a wide range of aromatic rings, including phenols, methoxy- and methylbenzenes, as an excellent way to produce aromatic aldehydes. Here we determine that the regioselectivity of this process is highly promoted by the coordination between the atoms present in the aromatic moiety and those in the metal core.

Synthesis of polyalkoxy-3-(4-methoxyphenyl)coumarins with antimitotic activity from plant allylpolyalkoxybenzenes

Tsyganov, Dmitry V.,Chernysheva, Natalia B.,Salamandra, Lev K.,Konyushkin, Leonid D.,Atamanenko, Olga P.,Semenova, Marina N.,Semenov, Victor V.

, p. 147 - 149 (2013/07/26)

Novel polyalkoxy-3-(4-methoxyphenyl)coumarins - analogues of natural antimitotic compounds - were synthesized from plant allylpolyalkoxybenzenes and tested in vivo in the phenotypic sea urchin embryo assay for antiproliferative antitubulin activity.

o-Formylation of electron-rich phenols with dichloromethyl methyl ether and TiCl4

García, Oscar,Nicolás, Ernesto,Albericio, Fernando

, p. 4961 - 4963 (2007/10/03)

o-Formylation of electron-rich phenols is accomplished with dichloromethyl methyl ether and TiCl4. The reaction gives excellent yields, good regioselectivity, and does not leading to diformylation.

Synthesis of 5,6'-Dihydroxy-6,7,2',3',4'-pentamethoxyflavone: Revision of Structure of Brickellin

Malhotra, Sunita,Sharma, V. K.,Gupta, S. R.,Parmar, V. S.

, p. 59 - 60 (2007/10/02)

5,6'-Dihydroxy-6,7,2',3',4'-pentamethoxyflavone (I), the constitution proposed for brickellin, a new highly oxygenated flavone isolated from Brickellia veronicaefolia and B. chlorolepsis (Phytochemistry 34 163) has been synthesised.The spectral dat

SYNTHESIS OF 5,6'-dihydroxy-2',3',4',6,7-PENTAMETHOXYFLAVONE

Iinuma, Munekazu,Iwashima, Kiyoshi,Tanaka, Toshiyuki,Matsuura, Shin

, p. 4217 - 4219 (2007/10/02)

5,6'-Dihydroxy-2',3',4',6,7-pentamethoxy- (1), 2',5-dihydroxy-3',4',6,6',7-pentamethoxy- (2) and 3',5-dihydroxy-2',4',6,6',7-pentamethoxyflavone (3) were synthesized to compare with brickellin isolated from Brickellia veronicaefolia and B. chlorolepis.The

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