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Benzeneacetic acid, a-methyl-4-[(2-oxocyclohexyl)methyl]-, commonly known as Pseudoephedrine, is a pharmaceutical drug that serves as a potent decongestant. It is primarily used to alleviate nasal congestion resulting from allergies, sinusitis, or the common cold. Pseudoephedrine operates by constricting the blood vessels in the nasal passages, thereby diminishing swelling and congestion. However, due to its chemical resemblance to amphetamines, it has been implicated in the illegal production of methamphetamine, leading to its regulation and restricted availability in pharmacies.

68767-16-8

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68767-16-8 Usage

Uses

Used in Pharmaceutical Industry:
Benzeneacetic acid, a-methyl-4-[(2-oxocyclohexyl)methyl]is utilized as a decongestant in the pharmaceutical industry to treat nasal congestion caused by various conditions such as allergies, sinusitis, or the common cold. Its effectiveness in reducing swelling and congestion makes it a popular choice for over-the-counter cold and allergy medications.
Used in Regulatory Measures:
Due to its potential use in the illegal production of methamphetamine, Benzeneacetic acid, a-methyl-4-[(2-oxocyclohexyl)methyl]has become a regulated substance. This regulatory measure aims to curb the misuse of pseudoephedrine in the production of illicit drugs while ensuring its continued availability for legitimate medical purposes. As a result, it is often only available behind the pharmacy counter, with restrictions on the quantity that can be purchased within a given time frame.

Check Digit Verification of cas no

The CAS Registry Mumber 68767-16-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,7,6 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 68767-16:
(7*6)+(6*8)+(5*7)+(4*6)+(3*7)+(2*1)+(1*6)=178
178 % 10 = 8
So 68767-16-8 is a valid CAS Registry Number.

68767-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-[(2-oxocyclohexyl)methyl]phenyl]propanoic acid

1.2 Other means of identification

Product number -
Other names 2-(4-((2-Oxocyclohexyl)methyl)phenyl)propanoic acid

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:68767-16-8 SDS

68767-16-8Relevant academic research and scientific papers

Ophthalmic anti-inflammatory agents

-

, (2008/06/13)

Compounds of formula: STR1 (wherein R represents hydrogen or methyl, >A--B-- represents a >CH--CH2 -- or >C=CH-- group; >C--Z represents a >C=O or >CH--OH group; and n represents 1 or 2) and ophthalmically acceptable salts and esters thereof are useful as ophthalmic anti-inflammatory agents.

Synthesis and Antiinflammatory Activity of acetic Acids and Related Compounds

Terada, Atsusuke,Naruto, Shunji,Wachi, Kazuyuki,Tanaka, Shigeru,Iizuka, Yoshio,Misaka, Eiichi

, p. 212 - 216 (2007/10/02)

acetic acid derivatives and related compounds were synthesized to test their antiinflammatory and analgesic activities.Some of the compounds in this series were found to have good activity in the carrageenan edema test.Among them, sodium 2-phenyl>propionate dihydrate (15) and 2-phenyl>propionic acid (13b) showed potent analgesic and antiadjuvant arthritis activities with excellent antipyretic properties.

Substituted phenylacetic acid derivatives and process for the preparation thereof

-

, (2008/06/13)

4-(2-Oxo- or hydroxyimino-cycloalkan-1-ylmethyl)phenylacetic acid derivative and nontoxic pharmaceutically acceptable salt thereof are useful as an anti-inflammatory agent. The above 2-oxo-compound may be prepared by (a) hydrolyzing and decarboxylating 4-(1-alkoxycarbonyl-2-oxocycloalkan-1-ylmethyl)phenylacetic acid ester derivative or (b) reacting p-halomethylphenylacetic acid ester derivative with an enamine of cycloalkanone and hydrolyzing the resulting product. And further, the above 2-hydroxyimino-compound may be prepared by (c) reacting 4-(2-oxocycloalkan-1-ylmethyl)phenylacetic acid derivative (the product of process (a) or (b)) with hydroxylamine or (d) reacting a dilithium salt of cycloalkanone oxime with p-halomethyl- or p-sulfonyloxymethyl-phenylacetic acid ester derivative and hydrolyzing the resulting product.

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