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Benzenepropanoic acid, α-(4-chlorophenoxy)-, also known as 2-(4-chlorophenoxy)propionic acid or 2-(4-chlorophenoxy)propanoic acid, is an organic compound with the chemical formula C9H9ClO3. It is a derivative of benzenepropanoic acid, featuring a 4-chlorophenoxy group attached to the α-carbon. Benzenepropanoic acid, a-(4-chlorophenoxy)- is a white crystalline solid and is soluble in water, ethanol, and acetone. It is primarily used as a plant growth regulator and herbicide, specifically in the control of broadleaf weeds and grasses in various crops. Due to its chemical structure and properties, it can interfere with plant hormone signaling, leading to uncontrolled growth and ultimately plant death.

4687-20-1

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4687-20-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4687-20-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,8 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4687-20:
(6*4)+(5*6)+(4*8)+(3*7)+(2*2)+(1*0)=111
111 % 10 = 1
So 4687-20-1 is a valid CAS Registry Number.

4687-20-1Relevant 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.

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