Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2-CHLORO-6-METHOXYNICOTINIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

503000-87-1 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 503000-87-1 Structure
  • Basic information

    1. Product Name: 2-CHLORO-6-METHOXYNICOTINIC ACID
    2. Synonyms: 2-CHLORO-6-METHOXYNICOTINIC ACID;2-Chloro-6-methoxypyridine-3-carboxylic acid;2-Chloro-6-methoxypyridine-3-carboxylic acid, 3-Carboxy-2-chloro-6-methoxypyridine
    3. CAS NO:503000-87-1
    4. Molecular Formula: C7H6ClNO3
    5. Molecular Weight: 187.58
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 503000-87-1.mol
  • Chemical Properties

    1. Melting Point: 231-234℃
    2. Boiling Point: 310.391 °C at 760 mmHg
    3. Flash Point: 141.52 °C
    4. Appearance: /
    5. Density: 1.43 g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.567
    8. Storage Temp.: Inert atmosphere,Room Temperature
    9. Solubility: N/A
    10. PKA: 2.41±0.28(Predicted)
    11. CAS DataBase Reference: 2-CHLORO-6-METHOXYNICOTINIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-CHLORO-6-METHOXYNICOTINIC ACID(503000-87-1)
    13. EPA Substance Registry System: 2-CHLORO-6-METHOXYNICOTINIC ACID(503000-87-1)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 503000-87-1(Hazardous Substances Data)

503000-87-1 Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 46, p. 702, 2003 DOI: 10.1021/jm020270n

Check Digit Verification of cas no

The CAS Registry Mumber 503000-87-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,0,0 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 503000-87:
(8*5)+(7*0)+(6*3)+(5*0)+(4*0)+(3*0)+(2*8)+(1*7)=81
81 % 10 = 1
So 503000-87-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClNO3/c1-12-5-3-2-4(7(10)11)6(8)9-5/h2-3H,1H3,(H,10,11)

503000-87-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H34001)  2-Chloro-6-methoxynicotinic acid, 95%   

  • 503000-87-1

  • 250mg

  • 410.0CNY

  • Detail
  • Alfa Aesar

  • (H34001)  2-Chloro-6-methoxynicotinic acid, 95%   

  • 503000-87-1

  • 1g

  • 1142.0CNY

  • Detail
  • Aldrich

  • (ADE000607)  2-Chloro-6-methoxynicotinic acid  AldrichCPR

  • 503000-87-1

  • ADE000607-1G

  • 7,411.95CNY

  • Detail

503000-87-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-6-methoxynicotinic acid

1.2 Other means of identification

Product number -
Other names 2-Chloro-6-methoxypyridine-3-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:503000-87-1 SDS

503000-87-1Relevant articles and documents

Structure-Guided Optimization of HIV Integrase Strand Transfer Inhibitors

Zhao, Xue Zhi,Smith, Steven J.,Maskell, Daniel P.,Métifiot, Mathieu,Pye, Valerie E.,Fesen, Katherine,Marchand, Christophe,Pommier, Yves,Cherepanov, Peter,Hughes, Stephen H.,Burke, Terrence R.

, p. 7315 - 7332 (2017)

Integrase mutations can reduce the effectiveness of the first-generation FDA-approved integrase strand transfer inhibitors (INSTIs), raltegravir (RAL) and elvitegravir (EVG). The second-generation agent, dolutegravir (DTG), has enjoyed considerable clinical success; however, resistance-causing mutations that diminish the efficacy of DTG have appeared. Our current findings support and extend the substrate envelope concept that broadly effective INSTIs can be designed by filling the envelope defined by the DNA substrates. Previously, we explored 1-hydroxy-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxamides as an INSTI scaffold, making a limited set of derivatives, and concluded that broadly effective INSTIs can be developed using this scaffold. Herein, we report an extended investigation of 6-substituents as well the first examples of 7-substituted analogues of this scaffold. While 7-substituents are not well-tolerated, we have identified novel substituents at the 6-position that are highly effective, with the best compound (6p) retaining better efficacy against a broad panel of known INSTI resistant mutants than any analogues we have previously described.

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

-

Page/Page column 63-64, (2020/06/01)

Compounds and pharmaceutically acceptable salts thereof, and compositions and methods for treating human immunodeficiency virus (HIV) infection are set forth.

Design of Development Candidate eFT226, a First in Class Inhibitor of Eukaryotic Initiation Factor 4A RNA Helicase

Ernst, Justin T.,Thompson, Peggy A.,Nilewski, Christian,Sprengeler, Paul A.,Sperry, Samuel,Packard, Garrick,Michels, Theodore,Xiang, Alan,Tran, Chinh,Wegerski, Christopher J.,Eam, Boreth,Young, Nathan P.,Fish, Sarah,Chen, Joan,Howard, Haleigh,Staunton, Jocelyn,Molter, Jolene,Clarine, Jeff,Nevarez, Andres,Chiang, Gary G.,Appleman, Jim R.,Webster, Kevin R.,Reich, Siegfried H.

supporting information, p. 5879 - 5955 (2020/07/03)

Dysregulation of protein translation is a key driver for the pathogenesis of many cancers. Eukaryotic initiation factor 4A (eIF4A), an ATP-dependent DEAD-box RNA helicase, is a critical component of the eIF4F complex, which regulates cap-dependent protein synthesis. The flavagline class of natural products (i.e., rocaglamide A) has been shown to inhibit protein synthesis by stabilizing a translation-incompetent complex for select messenger RNAs (mRNAs) with eIF4A. Despite showing promising anticancer phenotypes, the development of flavagline derivatives as therapeutic agents has been hampered because of poor drug-like properties as well as synthetic complexity. A focused effort was undertaken utilizing a ligand-based design strategy to identify a chemotype with optimized physicochemical properties. Also, detailed mechanistic studies were undertaken to further elucidate mRNA sequence selectivity, key regulated target genes, and the associated antitumor phenotype. This work led to the design of eFT226 (Zotatifin), a compound with excellent physicochemical properties and significant antitumor activity that supports clinical development.

INHIBITORS OF FIBROBLAST ACTIVATION PROTEIN

-

Paragraph 0728-0731; 0798-0801, (2019/07/03)

Compounds and compositions for modulating fibroblast activation protein (FAP) are described. The compounds and compositions may find use as therapeutic agents for the treatment of diseases, including hyperproliferative diseases.

Halogenated allyl amine type SSAO/VAP-1 inhibitor and application thereof

-

Paragraph 0315; 0319-0321, (2019/06/08)

The invention belongs to the technical field of medicine, and particularly relates to a halogenated allyl amine type compound shown as a formula I, medically acceptable salt, ester or stereo isomers thereof, wherein R1, R2, R3, R4, R5, R6, L1, Cy1, R7 and p are defined in description. The invention also relates to a medicine preparation containing the compounds, a medicine composition containing the compounds, and application of the compounds to prevention and/or treatment on diseases relevant to SSAO/VAP 1 protein or diseases caused by SSAO/VAP 1 protein mediating. The formula I is shown in the description.

ARYLCARBOXAMIDES AND USES THEREOF

-

Paragraph 0278, (2017/12/13)

The present disclosure is directed to compounds of formula (I): or a pharmaceutically acceptable salt, solvate or solvate of the salt thereof. Compounds of formula (I) are inhibitors of NOX4 and are useful in the treatment of fibrotic diseases such as scleroderma; lung disease, such as pulmonary fibrosis including idiopathic pulmonary fibrosis (IPF); heart disease, such as heart failure due to ischaemic heart disease, valvular heart disease and hypertensive heart disease, diabetic cardiomyopathy and hypertension; liver disease, such as cirrhosis of the liver; and kidney disease, such as progressive kidney disease glomerulonephritis and diabetic nephropathy; and eye disease such as diabetic retinopathy; skin or subcutaneous scarring, such as keloids, adhesions, hypertrophic scarring or cosmetic scarring; or as an adjuvant or anti-fibrotic in pancreatic cancer to increase chemotherapeutic drug penetration by reducing the density of the connective tissue stroma.

EIF4A-INHIBITING COMPOUNDS AND METHODS RELATED THERETO

-

Paragraph 0684; 0685, (2017/08/01)

The present invention provides synthesis, pharmaceutically acceptable formulations and uses of compounds in accordance with Formula I, or a stereoisomer, tautomer or pharmaceutically acceptable salt thereof. For Formula I compounds X, Y, R1, R2, R3a, R3b, R4a, R4b and R5 are as defined in the specification. The inventive Formula I compounds are inhibitors of eIF4A and find utility in any number of therapeutic applications, including but not limited to treatment of inflammation and various cancers.

AROMATIC COMPOUND

-

Paragraph 1367; 1368, (2016/05/19)

Provided is a novel aromatic ring compound having a GPR40 agonist activity and a GLP-1 secretagogue action. A compound represented by the formula: wherein each symbol is as described in the DESCRIPTION, or a salt thereof has a GPR40 agonist activity and a GLP-1 secretagogue action, is useful for the prophylaxis or treatment of cancer, obesity, diabetes, hypertension, hyperlipidemia, cardiac failure, diabetic complications, metabolic syndrome, sarcopenia and the like, and affords superior efficacy.

THIOARYL DERIVATIVES AS GPR120 AGONISTS

-

Paragraph 752-754, (2014/05/24)

The present invention relates to thioaryl derivatives of Formula 1 as defined in the specification, a method for preparing the same, a pharmaceutical composition comprising the same and use thereof. The thioaryl derivatives of Formula 1 according to the present invention promote GLP-1 formation in the gastrointestinal tract and improve insulin resistance in macrophages, pancreas cells, etc. due to anti-inflammatory action, and can accordingly be effectively used for preventing or treating diabetes, complications of diabetes, inflammation, obesity, non-alcoholic fatty liver, steatohepatitis or osteoporosis.

COMPOUNDS FOR TREATING SPINAL MUSCULAR ATROPHY

-

Paragraph 00931; 00932, (2013/09/12)

Provided herein are compounds, compositions thereof and uses therewith for treating spinal muscular atrophy.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 503000-87-1