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3507-48-0

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3507-48-0 Usage

General Description

2-Benzothiazolecarboxylicacid, 4-methoxy-(7CI,8CI,9CI) is a chemical compound with the molecular formula C10H9NO3S. It is a derivative of benzothiazole and carboxylic acid, and it contains a methoxy group. 2-Benzothiazolecarboxylicacid,4-methoxy-(7CI,8CI,9CI) is used in various chemical reactions and organic synthesis processes. It is also used as an intermediate in the manufacturing of pharmaceuticals and agrochemicals. Additionally, it has potential applications in the development of new materials and compounds. The exact properties and uses of this chemical may vary depending on the specific application and formulation.

Check Digit Verification of cas no

The CAS Registry Mumber 3507-48-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,0 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3507-48:
(6*3)+(5*5)+(4*0)+(3*7)+(2*4)+(1*8)=80
80 % 10 = 0
So 3507-48-0 is a valid CAS Registry Number.

3507-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxy-1,3-benzothiazole-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Benzothiazolecarboxylicacid,4-methoxy

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:3507-48-0 SDS

3507-48-0Relevant articles and documents

Lysophosphatidic acid receptor antagonists and preparation method thereof

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Paragraph 0709-0710; 0718-0720, (2020/07/29)

The invention belongs to the technical field of medicinal chemistry, and particularly relates to lysophosphatidic acid receptor antagonists and a preparation method thereof. The applicant surprisinglyfinds that compounds provided by the invention have high LPAR1 antagonistic activity and selectivity, low toxicity, good metabolic stability and good drug development prospect, and can be used for preventing or treating diseases or symptoms related to LPAR1. The applicant also accidentally finds that the IC50 value of part of the compounds can be as low as 300 nM or below and even 50 nM or below.Moreover, the compounds disclosed by the invention have better safety, and the CC50 range of the compounds can reach 200 [mu]M or above. In addition, the compounds of the present invention have goodmetabolic stability in humans, rats, and mice, such excellent inhibitory activity being very desirable for their use as LPAR1 inhibitors in the above diseases or disorders. In addition, the preparation method of the compounds is simple, mild in reaction condition, high in product yield and suitable for industrial production.

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