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2-amino-3-(benzyloxy)-4-methylbenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28649-39-0

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28649-39-0 Usage

General Description

2-amino-3-(benzyloxy)-4-methylbenzoic acid is an organic compound with a molecular formula C16H15NO3 and a molar mass of 269.29 g/mol. It is a derivative of benzoic acid, with an amino group and a benzyloxy group attached to the aromatic ring. The presence of the methyl group further modifies the chemical properties of the compound. This chemical is commonly used in the pharmaceutical industry as a precursor for the synthesis of various drugs. It has also been studied for its potential anticancer and anti-inflammatory properties. The compound's structure and properties make it a versatile building block for the synthesis of various organic compounds and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 28649-39-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,6,4 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 28649-39:
(7*2)+(6*8)+(5*6)+(4*4)+(3*9)+(2*3)+(1*9)=150
150 % 10 = 0
So 28649-39-0 is a valid CAS Registry Number.

28649-39-0SDS

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 2-amino-4-methyl-3-phenylmethoxybenzoic acid

1.2 Other means of identification

Product number -
Other names 2-Amino-3-benzyloxy-4-methyl-benzoesaeure

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:28649-39-0 SDS

28649-39-0Relevant academic research and scientific papers

SYNTHESIS OF HYBRID TILIVALLINES AND THEIR 11-CYANO ANALOGS

Matsunaga, Nobuyuki,Aoyama, Toyohiko,Shioiri, Takayuki

, p. 387 - 400 (2007/10/02)

Hybrid tilivallines (4), derived from tilivalline (1a) and anthramycin (2) or tomaymycin (3), and their 11-cyano analogs (15) have been efficiently synthesized from the acetal amides (7a, b) : the key step is an intramolecular Mannich type cyclization acc

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