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56724-03-9

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56724-03-9 Usage

Description

3-Methoxy-2-methylbenzaldehyde, also known as isosafrole aldehyde, is an organic compound with the molecular formula C9H10O2. It is an aromatic aldehyde derived from the safrole family, characterized by its distinct chemical structure and functional groups. 3-METHOXY-2-METHYL-BENZALDEHYDE is known for its unique chemical properties and potential applications in various industries.

Uses

Used in Pharmaceutical Industry:
3-Methoxy-2-methylbenzaldehyde is used as a reagent for the synthesis of benzosuberebe-based inhibitors of tubulin polymerization. Tubulin polymerization is a crucial process in cell division, and inhibiting this process can lead to the prevention of cancer cell growth. As a result, this compound plays a significant role in the development of novel anticancer drugs.

Synthesis Reference(s)

The Journal of Organic Chemistry, 54, p. 3730, 1989 DOI: 10.1021/jo00276a041

Check Digit Verification of cas no

The CAS Registry Mumber 56724-03-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,7,2 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56724-03:
(7*5)+(6*6)+(5*7)+(4*2)+(3*4)+(2*0)+(1*3)=129
129 % 10 = 9
So 56724-03-9 is a valid CAS Registry Number.

56724-03-9SDS

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 3-methoxy-2-methylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 3-Methoxy-2-methylbenzaldehyd

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:56724-03-9 SDS

56724-03-9Relevant articles and documents

Vanadium-Catalyzed Oxidative Intramolecular Coupling of Tethered Phenols: Formation of Phenol-Dienone Products

Gilmartin, Philip H.,Kozlowski, Marisa C.

supporting information, p. 2914 - 2919 (2020/04/10)

A mild and efficient method for the vanadium-catalyzed intramolecular coupling of tethered free phenols is described. The corresponding phenol-dienone products are prepared directly in good yields with low catalyst loadings. Electronically diverse tethered phenol precursors are well tolerated, and the catalytic method was effectively applied as the key step in syntheses of three natural products and a synthetically useful morphinan alkaloid precursor.

Hydrazide-Catalyzed Polyene Cyclization: Asymmetric Organocatalytic Synthesis of cis-Decalins

Plamondon, Samuel J.,Warnica, Josephine M.,Kaldre, Dainis,Gleason, James L.

supporting information, p. 253 - 258 (2019/11/28)

Polyene cyclizations offer rapid entry into terpenoid ring systems. Although enantioselective cyclizations of (E)-polyenes to form trans-decalin ring systems are well precedented, highly enantioselective cyclizations of (Z)-polyenes to form the correspond

Volatiles from the xylarialean fungus Hypoxylon invadens

Dickschat, Jeroen S.,Wang, Tao,Stadler, Marc

, p. 734 - 746 (2018/04/16)

The volatiles emitted by agar plate cultures of the xylarialean fungus Hypoxylon invadens were investigated by use of a closed loop stripping apparatus in combination with GC-MS. Several aromatic compounds were found that could only be identified by comparison to all possible constitutional isomers with different ring substitution patterns. For the set of identified compounds a plausible biosynthetic scheme was suggested that gives further support for the assigned structures.

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