Welcome to LookChem.com Sign In|Join Free
  • or
2-(4-(Thiomethyl)phenoxy)propionic acid is a chemical compound with the molecular formula C10H12O3S. It is an organic acid derivative featuring a phenoxy group with a thiomethyl substituent at the para position, and a propionic acid chain attached to the 2-position. 2-<4-(thiomethyl)phenoxy>propionic acid is known for its potential applications in various fields, including pharmaceuticals and agrochemicals, where it may serve as a building block for the synthesis of more complex molecules. Its structure provides a unique combination of functional groups that can participate in a range of chemical reactions, making it a versatile intermediate in organic synthesis.

3364-90-7

Post Buying Request

3364-90-7 Suppliers

Recommended suppliers

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

3364-90-7 Usage

Properties

1. Chemical formula: C11H12O3S
2. Molecular weight: 224.28 g/mol
3. Appearance: Colorless to light yellow liquid
4. Odor: Characteristic aromatic odor
5. Solubility: Soluble in organic solvents

Specific content

1. Propionic acid core
2. Phenoxy group
3. Thiomethyl group
4. Used in industrial and agricultural applications
5. Building block for synthesis of organic compounds
6. Herbicide and fungicide in agriculture
7. Thiomethyl group enhances reactivity
8. Phenoxy group provides aromatic properties

Check Digit Verification of cas no

The CAS Registry Mumber 3364-90-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3364-90:
(6*3)+(5*3)+(4*6)+(3*4)+(2*9)+(1*0)=87
87 % 10 = 7
So 3364-90-7 is a valid CAS Registry Number.

3364-90-7Downstream Products

3364-90-7Relevant academic research and scientific papers

Presynaptic cholinergic modulators as potent cognition enhancers and analgesic drugs. 2. 2-Phenoxy-, 2-(phenylthio)-, and 2-(phenylamino)alkanoic acid esters

Gualtieri,Bottalico,Calandrella,Dei,Giovannoni,Mealli,Romanelli,Scapecchi,Teodori,Galeotti,Ghelardini,Giotti,Bartolini

, p. 1712 - 1719 (2007/10/02)

Further modifications of the leads ((R)-(+)-hyoscyamine and (p- chlorophenyl)propionic acid α-tropanyl ester), which show analgesic and nootropic activities as a consequence of increased central presynaptic ACh release, are reported. 2-Phenoxy- and 2-(phenylthio)alkanoic acid esters showed the best results. Several members of these classes possess analgesic properties which are comparable to that of morphine and at the same time are able to reverse dicyclomine-induced amnesia. Confirmation was found that the mechanism of action is due to an increase in ACh release at central muscarinic synapses and that both auto- and heteroreceptors controlling ACh release are very likely involved. According to the results obtained with (R)- (+)-hyoscyamine, analgesic activity is stereochemistry dependent, since the R-(+)-enantiomers are always more efficacious than the corresponding S-(-)- ones. On the basis of their potency and acute toxicity, compounds (±)-28 (SM21) and (±)-42 (SM32) were selected for further study.

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 3364-90-7