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4-Hydroxy-7-methylnaphthalene-2-carboxylic acid is an organic compound with the molecular formula C12H10O3. It is a white crystalline solid that belongs to the class of naphthalene derivatives, specifically a hydroxylated and methylated naphthalene-2-carboxylic acid. 4-hydroxy-7-methylnaphthalene-2-carboxylic acid is characterized by the presence of a hydroxyl group at the 4-position, a methyl group at the 7-position, and a carboxylic acid group at the 2-position on the naphthalene ring. It is used in various applications, including the synthesis of pharmaceuticals and other organic compounds, due to its unique chemical structure and reactivity. The compound's properties, such as its solubility and stability, make it a valuable intermediate in the chemical industry.

24894-73-3

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24894-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24894-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,8,9 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24894-73:
(7*2)+(6*4)+(5*8)+(4*9)+(3*4)+(2*7)+(1*3)=143
143 % 10 = 3
So 24894-73-3 is a valid CAS Registry Number.

24894-73-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Hydroxy-7-methyl-2-naphthoic acid

1.2 Other means of identification

Product number -
Other names 4-hydroxy-7-methylnaphthalene-2-carboxylic acid

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:24894-73-3 SDS

24894-73-3Relevant academic research and scientific papers

Synthesis of 6-deoxymollugins and their inhibitory activities on tyrosinase

Liang, Jing Lu,Javed, Umair,Lee, Seung Ho,Park, Jae Gyu,Jahng, Yurngdong

, p. 862 - 872 (2014/08/05)

A series of 6-deoxymollugins were prepared five steps from benzaldehyde and its derivatives via phenylboronic acid-catalyzed chromenylation as a key step. Their inhibitory activities against tyrosinase from mushroom were evaluated to show that the parent,

FUSED-RING DERIVATIVE AND MEDICAL APPLICATION OF SAME

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Paragraph 0082, (2013/03/26)

The present invention provides compounds useful as agents for the prevention or treatment of a disease associated with abnormal plasma uric acid level and the like. The present invention relates to fused ring derivatives represented by the following formula (I) having xanthine oxidase inhibitory activities and useful as agents for the prevention or treatment of a disease associated with abnormality of plasma uric acid level, prodrugs thereof, salts thereof or the like. In the formula (I), X1 and X2 represent CH or N; ring U represents aryl or heteroaryl; m represents integral number from 0 to 2; n represents integral number from 0 to 3; R1 represents a hydroxy group, amino or C1-6 alkyl; R2 represents C1-6 alkyl, C1-6 alkoxy C1-6 alkyl or the like.

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