Welcome to LookChem.com Sign In|Join Free
  • or
4-methylidene-5-oxo-2-undecyltetrahydrofuran-3-carboxylic acid is a complex organic compound with the molecular formula C16H26O4. It is a derivative of tetrahydrofuran, a heterocyclic compound consisting of a five-membered ring with one oxygen atom and four carbon atoms. The structure of 4-methylidene-5-oxo-2-undecyltetrahydrofuran-3-carboxylic acid features a methylidene group (CH2) at the 4-position, an oxo group (C=O) at the 5-position, and an undecyl chain (C11H23) attached to the 2-position. The carboxylic acid group (COOH) is present at the 3-position, which gives the compound its acidic properties. This chemical is primarily used in the synthesis of various pharmaceuticals and other organic compounds due to its unique structure and reactivity.

570-13-8

Post Buying Request

570-13-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

570-13-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 570-13-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 570-13:
(5*5)+(4*7)+(3*0)+(2*1)+(1*3)=58
58 % 10 = 8
So 570-13-8 is a valid CAS Registry Number.

570-13-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylidene-5-oxo-2-undecyloxolane-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-Furancarboxylic acid,tetrahydro-4-methylene-5-oxo-2-undecyl

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:570-13-8 SDS

570-13-8Downstream Products

570-13-8Relevant academic research and scientific papers

Enzymatic resolution of α-methyleneparaconic acids and evaluation of their biological activity

Chakrabarty, Kuheli,Defrenza, Ivana,Denora, Nunzio,Drioli, Sara,Forzato, Cristina,Franco, Massimo,Lentini, Giovanni,Nitti, Patrizia,Pitacco, Giuliana

, p. 239 - 246 (2015/03/18)

Both enantiomers of three biologically relevant paraconic acids-MB-3, methylenolactocin, and C75-were obtained with enantioselectivities up to 99% by kinetic enzymatic resolutions. Good enantiomeric excesses were obtained for MB-3 and methylenolactocin, using α-chymotrypsin and aminoacylase as enantiocomplementary enzymes, while C75 was resolved with aminoacylase. They all were evaluated for their antiproliferative, antibacterial, and antifungal activities, showing weak effects and practically no difference between enantiomers in each case. At high concentrations (16-64μg/mL), (-)- C75 acted as an antimicrobial agent against Gram-positive bacteria.

Synthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactions

Kongsaeree, Palangpon,Meepowpan, Puttinan,Thebtaranonth, Yodhathai

, p. 1913 - 1922 (2007/10/03)

Both forms of the enantiomerically pure methylenolactocin, nephrosterinic and protolichesterinic acid have been synthesized via tandem aldol-lactonization reactions from corresponding optically active itaconate-anthracene adducts.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 570-13-8