Welcome to LookChem.com Sign In|Join Free

CAS

  • or
5-(benzyloxy)-4-hydroxypicolinic acid is a chemical compound with the molecular formula C13H11NO4. It is a derivative of picolinic acid, featuring a benzyloxy group and a hydroxyl group on the 4th and 5th carbon positions, respectively. 5-(benzyloxy)-4-hydroxypicolinic acid is known for its potential biological activities and is utilized in various scientific and medical applications.

107550-30-1 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 107550-30-1 Structure
  • Basic information

    1. Product Name: 5-(benzyloxy)-4-hydroxypicolinic acid
    2. Synonyms: 5-(benzyloxy)-4-hydroxypicolinic acid;3-Benzyloxy-4-pyridone-6-carboxylic acid;5-Benzyloxy-4-pyridone-2-carboxylic acid;O-Benzylcomenamic acid;5-(benzyloxy)-4-oxo-1,4-dihydropyridine-2-carboxylic acid;5-benzyloxy-4-oxo-1h-pyridine-2-carboxylic acid;2-Pyridinecarboxylic acid, 1,4-dihydro-4-oxo-5-(phenylmethoxy)-
    3. CAS NO:107550-30-1
    4. Molecular Formula: C13H11NO4
    5. Molecular Weight: 245.23074
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107550-30-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 475.6±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.37
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 0.53±0.20(Predicted)
    10. CAS DataBase Reference: 5-(benzyloxy)-4-hydroxypicolinic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-(benzyloxy)-4-hydroxypicolinic acid(107550-30-1)
    12. EPA Substance Registry System: 5-(benzyloxy)-4-hydroxypicolinic acid(107550-30-1)
  • 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: 107550-30-1(Hazardous Substances Data)

107550-30-1 Usage

Uses

Used in Organic Synthesis:
5-(benzyloxy)-4-hydroxypicolinic acid is used as a building block in organic synthesis for the creation of other bioactive compounds. Its unique structure allows for the development of new molecules with potential applications in various fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-(benzyloxy)-4-hydroxypicolinic acid is used as a starting material for the development of new drug molecules. Its potential biological activities make it a valuable candidate for further research and development.
Used in Anti-inflammatory Applications:
5-(benzyloxy)-4-hydroxypicolinic acid is used as an anti-inflammatory agent due to its ability to modulate inflammatory pathways. This property makes it a promising candidate for the treatment of various inflammatory conditions.
Used in Antitumor Applications:
5-(benzyloxy)-4-hydroxypicolinic acid is used as an antitumor agent, exhibiting potential inhibitory effects on tumor growth and progression. Its ability to target specific cellular processes involved in cancer development and spread makes it a valuable compound in oncology research.
Used in Enzyme Inhibition:
5-(benzyloxy)-4-hydroxypicolinic acid is used to inhibit certain enzymes, which can be beneficial in the treatment of various diseases. By targeting specific enzymes, this compound may help regulate biological processes and provide therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 107550-30-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,5,5 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 107550-30:
(8*1)+(7*0)+(6*7)+(5*5)+(4*5)+(3*0)+(2*3)+(1*0)=101
101 % 10 = 1
So 107550-30-1 is a valid CAS Registry Number.

107550-30-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-oxo-5-phenylmethoxy-1H-pyridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names F2158-0449

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:107550-30-1 SDS

107550-30-1Relevant articles and documents

Preparation, gram-negative antibacterial activity, and hydrolytic stability of novel siderophore-conjugated monocarbam diols

Flanagan, Mark E.,Brickner, Steven J.,Lall, Manjinder,Casavant, Jeffrey,Deschenes, Laura,Finegan, Steven M.,George, David M.,Granskog, Karl,Hardink, Joel R.,Huband, Michael D.,Hoang, Thuy,Lamb, Lucinda,Marra, Andrea,Mitton-Fry, Mark,Mueller, John P.,Mullins, Lisa M.,Noe, Mark C.,O'Donnell, John P.,Pattavina, David,Penzien, Joseph B.,Schuff, Brandon P.,Sun, Jianmin,Whipple, David A.,Young, Jennifer,Gootz, Thomas D.

scheme or table, p. 385 - 390 (2011/07/09)

A novel series of monocarbam compounds exhibiting promising antibacterial activity against multidrug resistant Gram-negative microorganisms is reported, along with the synthesis of one such molecule MC-1 (1). Also reported are structure-activity relationships associated with the in vitro and in vivo efficacy of 1 and related analogues in addition to the hydrolytic stability of such compounds and possible implications thereof.

MONOCARBAMS

-

Page/Page column 12-13, (2010/07/04)

The invention relates to compounds of formula (I): wherein R1, R2, R3, R4, Rs, and R6 as defined herein. The invention also relates to pharmaceutical compositions and methods of treating bacterial infections using compounds of formula (I)

The total synthesis of the natural product endothelin converting enzyme (ECE) inhibitor, WS75624 B

Patt, William C.,Massa, Mark A.

, p. 1297 - 1300 (2007/10/03)

The first total synthesis of WS75624 B, 1, an endothelin converting enzyme inhibitor produced in a fermentation broth of Saccharothrix sp. No. 75624 is reported herein. WS75624 B is synthesized in 14 steps from commercially available kojic acid, 2. The synthetic methodology allows for facile substitution at multiple sites on the molecule.

2-oxo-1-[[(substituted sulfonyl)amino]carbonyl]azetidines

-

, (2008/06/13)

Antibacterial activity is exhibited by 2-azetidinones having a 3-acylamino substituent and having an activating group in the 1-position of the formula STR1

1-(substituted phosphorous)-azetidinone antibacterials

-

, (2008/06/13)

Antibacterial activity is exhibited by 2-azetidinones having an acylamino substituent in the 3-position and having an activating group in the 1-position of the formula STR1

3-acylamino-2-oxo-1-azetidinesulfonic acids

-

, (2008/06/13)

Antibacterial activity is exhibited by 2-azetidinones activated in the 1-position with an --SO3 H group and having in the 3-position an acylamino group of the formula STR1

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 107550-30-1