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6-Chloro-5-hydroxy-nicotinic acid methyl ester, also known as Methyl 6-Chloro-5-hydroxynicotinate, is a synthetic intermediate with significant applications in the chemical and pharmaceutical industries. It is characterized by its chlorinated and hydroxyl functional groups, which contribute to its unique chemical properties and reactivity.

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  • 915107-30-1 Structure
  • Basic information

    1. Product Name: 6-Chloro-5-hydroxy-nicotinic acid methyl ester
    2. Synonyms: 6-Chloro-5-hydroxy-nicotinic acid methyl ester
    3. CAS NO:915107-30-1
    4. Molecular Formula: C7H6ClNO3
    5. Molecular Weight: 188
    6. EINECS: 604-604-1
    7. Product Categories: N/A
    8. Mol File: 915107-30-1.mol
  • Chemical Properties

    1. Melting Point: 142-143 °C(Solv: water (7732-18-5))
    2. Boiling Point: 383.796°C at 760 mmHg
    3. Flash Point: 185.914°C
    4. Appearance: /
    5. Density: 1.433g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.569
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    9. Solubility: N/A
    10. PKA: 3.61±0.10(Predicted)
    11. CAS DataBase Reference: 6-Chloro-5-hydroxy-nicotinic acid methyl ester(CAS DataBase Reference)
    12. NIST Chemistry Reference: 6-Chloro-5-hydroxy-nicotinic acid methyl ester(915107-30-1)
    13. EPA Substance Registry System: 6-Chloro-5-hydroxy-nicotinic acid methyl ester(915107-30-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 915107-30-1(Hazardous Substances Data)

915107-30-1 Usage

Uses

Used in Pharmaceutical Industry:
6-Chloro-5-hydroxy-nicotinic acid methyl ester is used as a synthetic intermediate for the production of 5-Hydroxy-Imidacloprid (H943220), a metabolite of Imidacloprid (I274990). Imidacloprid is an active ingredient in certain neuro-active insecticides, making this ester a crucial component in the development and synthesis of effective pest control agents.

Check Digit Verification of cas no

The CAS Registry Mumber 915107-30-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,1,0 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 915107-30:
(8*9)+(7*1)+(6*5)+(5*1)+(4*0)+(3*7)+(2*3)+(1*0)=141
141 % 10 = 1
So 915107-30-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClNO3/c1-12-7(11)4-2-5(10)6(8)9-3-4/h2-3,10H,1H3

915107-30-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 6-chloro-5-hydroxynicotinate

1.2 Other means of identification

Product number -
Other names 2-Pyridinecarboxylic acid,6-chloro-5-formyl-,methyl ester

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:915107-30-1 SDS

915107-30-1Relevant articles and documents

Synthesis method of imidacloprid metabolite 5-hydroxyimidacloprid

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Paragraph 0053-0058; 0079-0084; 0097-0102, (2021/07/28)

The invention discloses a synthesis method of an imidacloprid metabolite 5-hydroxyimidacloprid, and belongs to the field of medicine synthesis. According to the synthesis method, methyl 5-hydroxynicotinate is used as a raw material, synthesis of the imidacloprid metabolite 5-hydroxylimidacloprid is achieved for the first time through six-step reaction, an optimal synthesis route and reaction conditions are screened out through a large number of experiments, the purity of the prepared target product can reach 99% or above, and the target product does not contain raw material medicine imidacloprid can be used for research on pharmacokinetics, raw material medicine impurity identification, environment control and protection and the like, provides a sample for impurity identification of imidacloprid, metabolic mechanism research, influence on the environment after medicine use, how to carry out corresponding protection and the like, and has important application value.

CHEMICAL COMPOUNDS

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Paragraph 00622; 00623; 00625; 00627; 00628, (2019/04/27)

Compounds of Formula (I), specifically hepatitis B virus and/or hepatitis D virus inhibitors, more specifically compounds that inhibit HBe antigen and HBs antigen in a subject, for the treatment of viral infections, and methods of preparing and using such compounds.

HETEROAROMATIC COMPOUNDS AS VANIN INHIBITORS

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Paragraph 0327; 0328, (2019/01/04)

The present invention encompasses compounds of the formula (I) wherein the groups A and B are defined herein, which are suitable for the treatment of diseases related to Vanin, and processes for making these compounds, pharmaceutical preparations containi

TBK/IKK INHIBITOR COMPOUNDS AND USES THEREOF

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Paragraph 0493; 0494, (2017/01/23)

The present invention relates to compounds of Formula I and pharmaceutically acceptable compositions thereof, useful as TBK/IKKε inhibitors.

AROMATIC RING COMPOUND

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Paragraph 0484; 0485, (2015/01/18)

Provided is an aromatic ring compound having a GPR40 agonist activity. A compound represented by the formula (I): wherein each symbol is as described in the DESCRIPTION, or a salt thereof has a GPR40 agonist activity, and is useful as an agent for the prophylaxis or treatment of diabetes and the like.

The design and synthesis of indazole and pyrazolopyridine based glucokinase activators for the treatment of Type 2 diabetes mellitus

Pfefferkorn, Jeffrey A.,Tu, Meihua,Filipski, Kevin J.,Guzman-Perez, Angel,Bian, Jianwei,Aspnes, Gary E.,Sammons, Matthew F.,Song, Wei,Li, Jian-Cheng,Jones, Christopher S.,Patel, Leena,Rasmusson, Tim,Zeng, Dongxiang,Karki, Kapil,Hamilton, Michael,Hank, Richard,Atkinson, Karen,Litchfield, John,Aiello, Robert,Baker, Levenia,Barucci, Nicole,Bourassa, Patricia,Bourbounais, Francis,D'Aquila, Theresa,Derksen, David R.,MacDougall, Margit,Robertson, Alan

, p. 7100 - 7105 (2013/01/15)

Glucokinase activators represent a promising potential treatment for patients with Type 2 diabetes. Herein, we report the identification and optimization of a series of novel indazole and pyrazolopyridine based activators leading to the identification of 4-(6-(azetidine-1-carbonyl)-5-fluoropyridin-3- yloxy)-2-ethyl-N-(5-methylpyrazin-2-yl)-2H-indazole-6-carboxamide (42) as a potent activator with favorable preclinical pharmacokinetic properties and in vivo efficacy.

NOVEL HETEROARYL IMIDAZOLES AND HETEROARYL TRIAZOLES AS GAMMA-SECRETASE MODULATORS

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Page/Page column 43, (2011/05/06)

Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula I; (I) as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

BIS-(SULFONYLAMINO) DERIVATIVES IN THERAPY 065

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Page/Page column 65, (2009/05/28)

The invention provides compounds of formula wherein R1, R2, R3, A and m are as defined in the specification and optical isomers, racemates and tautomers thereof, and pharmaceutically acceptable salts thereof; together with processes for their preparation, pharmaceutical compositions containing them and their use in therapy. The compounds are inhibitors of microsomal prostaglandin E synthase-1

BIS-(SULFONYLAMINO) DERIVATIVES IN THERAPY 066

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Page/Page column 137, (2009/06/27)

The invention provides compounds of formula wherein R1, R3, L1, L2, G1, G2, A and m are as defined in the specification and optical isomers, racemates and tautomers thereof, and pharmaceutically acceptable salts thereof; together with processes for their preparation, pharmaceutical compositions containing them and their use in therapy. The compounds are inhibitors of microsomal prostaglandin E synthase-1.

Multi-substituted pyridyl sulfoximines and their use as insecticides

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Page/Page column 9-10, (2008/12/04)

Multi-substituted pyridyl sulfoximines are useful as insecticides.

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