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Acetamide, N-methyl-N-(1-methyl-2-phenylethyl)-, also known as methyldesorphine, is a synthetic opioid analgesic drug structurally related to fentanyl. It acts as a potent agonist at the μ-opioid receptor, exhibiting similar effects to morphine and fentanyl. This chemical compound is primarily used in scientific research to study the mechanisms of opioid receptor activation and aid in the development of new pain-relieving medications.

27765-80-6

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27765-80-6 Usage

Uses

Used in Scientific Research:
Acetamide, N-methyl-N-(1-methyl-2-phenylethyl)is used as a research compound for understanding the mechanisms of opioid receptor activation and exploring the development of new pain-relieving medications.
Used in Pharmaceutical Development:
In the pharmaceutical industry, Acetamide, N-methyl-N-(1-methyl-2-phenylethyl)serves as a key component in the research and development of novel opioid analgesics, aiming to improve their efficacy and safety while minimizing the risk of addiction and abuse.

Check Digit Verification of cas no

The CAS Registry Mumber 27765-80-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,7,6 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27765-80:
(7*2)+(6*7)+(5*7)+(4*6)+(3*5)+(2*8)+(1*0)=146
146 % 10 = 6
So 27765-80-6 is a valid CAS Registry Number.

27765-80-6SDS

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 N-methyl-N-(1-phenylpropan-2-yl)acetamide

1.2 Other means of identification

Product number -
Other names Methamphetamine acetylated

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:27765-80-6 SDS

27765-80-6Downstream Products

27765-80-6Relevant articles and documents

Iron Hydride Radical Reductive Alkylation of Unactivated Alkenes

Saladrigas, Mar,Bonjoch, Josep,Bradshaw, Ben

supporting information, p. 684 - 688 (2020/01/31)

Iron-catalyzed hydrogen atom transfer-mediated intermolecular C-C coupling reactions between alkenes and tosylhydrazones, followed by in situ cleavage of the tosylhydrazine intermediates using Et3N, are described. The process involves a new strategic bond disconnection resulting in the reductive alkylation of nonactivated alkenes. The reaction is operationally simple, proceeds under mild conditions, and has a wide substrate scope.

Characterization of route specific impurities found in methamphetamine synthesized by the Leuckart and reductive amination methods

Kunalan, Vanitha,Daeid, Niamh Nic,Kerr, William J.,Buchanan, Hilary A. S.,McPherson, Allan R.

experimental part, p. 7342 - 7348 (2010/04/06)

Impurity profiling of seized methamphetamine can provide very useful information in criminal investigations and, specifically, on drug trafficking routes, sources of supply, and relationships between seizures. Particularly important is the identification of "route specific" impurities or those which indicate the synthetic method used for manufacture in illicit laboratories. Previous researchers have suggested impurities which are characteristic of the Leuckart and reductive amination (Al/Hg) methods of preparation. However, to date and importantly, these two synthetic methods have not been compared in a single study utilizing methamphetamine hydrochloride synthesized in-house and, therefore, of known synthetic origin. Using the same starting material, 1-phenyl-2-propanone (P2P), 40 batches of methamphetamine hydrochloride were synthesized by the Leuckart and reductive amination methods (20 batches per method). Both basic and acidic impurities were extracted separately and analyzed by GC/MS. From this controlled study, two route specific impurities for the Leuckart method and one route specific impurity for the reductive amination method are reported. The intra- and inter-batch variation of these route specific impurities was assessed. Also, the variation of the "target impurities" recently recommended for methamphetamine profiling is discussed in relation to their variation within and between production batches synthesized using the Leuckart and reductive amination routes.

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