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30766-22-4

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30766-22-4 Usage

Description

Methyl 5-hydroxynicotinate is an organic compound that serves as an intermediate in the synthesis of various pharmaceuticals. It is characterized by its light beige powder and lumps appearance.

Uses

Used in Pharmaceutical Industry:
Methyl 5-hydroxynicotinate is used as an intermediate for the preparation of selective cyclooxygenase-2 (COX-2) inhibitors. These inhibitors are important in the development of anti-inflammatory and pain-relieving medications, as they help reduce inflammation and pain without causing the side effects associated with non-selective COX inhibitors.
Additionally, Methyl 5-hydroxynicotinate is used as an intermediate to prepare imino sugars, which act as inhibitors of liver glycogen phosphorylase. This application is significant in the development of treatments for metabolic disorders and conditions related to glucose metabolism, such as diabetes and hypoglycemia.

Check Digit Verification of cas no

The CAS Registry Mumber 30766-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,6 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 30766-22:
(7*3)+(6*0)+(5*7)+(4*6)+(3*6)+(2*2)+(1*2)=104
104 % 10 = 4
So 30766-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO3/c1-11-7(10)5-2-6(9)4-8-3-5/h2-4,9H,1H3

30766-22-4 Well-known Company Product Price

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  • Aldrich

  • (689246)  Methyl5-hydroxy-3-pyridinecarboxylate  97%

  • 30766-22-4

  • 689246-1G

  • 1,510.47CNY

  • Detail
  • Aldrich

  • (689246)  Methyl5-hydroxy-3-pyridinecarboxylate  97%

  • 30766-22-4

  • 689246-5G

  • 6,280.56CNY

  • Detail

30766-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-hydroxypyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 5-hydroxynicotinate

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:30766-22-4 SDS

30766-22-4Relevant articles and documents

Synthesis and biological evaluation of a series of novel pyridinecarboxamides as potential multi-receptor antipsychotic drugs

Xu, Mingshuo,Wang, Yu,Yang, Feipu,Wu, Chunhui,Wang, Zhen,Ye, Bin,Jiang, Xiangrui,Zhao, Qingjie,Li, Jianfeng,Liu, Yongjian,Zhang, Junchi,Tian, Guanghui,He, Yang,Shen, Jingshan,Jiang, Hualiang

supporting information, p. 606 - 611 (2018/02/06)

In previous study, a series of benzamides was identified as potent antipsychotic agents. As a continuation of the program to discover novel antipsychotics, herein we reported the evaluation of a series of pyridinecarboxamide derivatives. The most promising compound 7h not only held good activities on dopamine D2, serotonin 5-HT1A and 5-HT2A receptors, but also exhibited low potency for α1A, H1 and 5-HT2C receptors, indicating a low propensity of side effects like orthostatic hypotension and weight gain. Furthermore, 7h exhibited more potent antipsychotic-like effect than aripiprazole in behavioral studies. The preliminary results were promising enough for further research around this scaffold.

MODIFIED COMPOUND OF ANDROGRAPHOLIDE

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Paragraph 0236-0238, (2019/01/04)

The present disclosure discloses a modified compound of andrographolide, and particularly discloses a compound shown in formula (I) and (II) or a pharmaceutically acceptable salt thereof.

SUBSTITUTED [1,2,4] TRIAZOLO [1,5-A] PYRIMIDIN-7-YL COMPOUNDS AS PDE2 INHIBITORS

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Page/Page column 52, (2015/11/10)

The invention provides a chemical entity of Formula (I): wherein R1, R2, X, Y and Z have any of the values described herein, and compositions comprising such chemical entities; methods of making them; and their use in a wide range of

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