Welcome to LookChem.com Sign In|Join Free
  • or
Methyl tetrahydro-5-methyl-4-oxo-3-furoate is a chemical compound with the molecular formula C7H10O4. It is a derivative of furoic acid, featuring a furan ring with a methyl group at the 5-position and a carboxymethyl group at the 3-position. methyl tetrahydro-5-methyl-4-oxo-3-furoate is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain antibiotics and antifungal agents. Its structure provides a versatile platform for further chemical modifications, making it a valuable component in organic synthesis.

3210-57-9

Post Buying Request

3210-57-9 Suppliers

Recommended suppliers

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

3210-57-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3210-57-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,1 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3210-57:
(6*3)+(5*2)+(4*1)+(3*0)+(2*5)+(1*7)=49
49 % 10 = 9
So 3210-57-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O4/c1-4-6(8)5(3-11-4)7(9)10-2/h4-5H,3H2,1-2H3

3210-57-9SDS

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 5-methyl-4-oxooxolane-3-carboxylate

1.2 Other means of identification

Product number -
Other names 3-Furancarboxylic acid,tetrahydro-5-methyl-4-oxo-,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:3210-57-9 SDS

3210-57-9Relevant academic research and scientific papers

NAD(P)h-independent asymmetric C=C bond reduction catalyzed by ene reductases by using artificial co-substrates as the hydrogen donor

Winkler, Christoph K.,Clay, Dorina,Entner, Marcello,Plank, Markus,Faber, Kurt

, p. 1403 - 1409 (2014/04/03)

To develop a nicotinamide-independent single flavoenzyme system for the asymmetric bioreduction of C=C bonds, four types of hydrogen donor, encompassing more than 50 candidates, were investigated. Six highly potent, cheap, and commercially available co-substrates were identified that (under the optimized conditions) resulted in conversions and enantioselectivities comparable with, or even superior to, those obtained with traditional two-enzyme nicotinamide adenine dinucleotide phosphate (NAD(P)H)-recycling systems.

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 3210-57-9