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27765-80-6

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27765-80-6 Usage

General Description

Acetamide, N-methyl-N-(1-methyl-2-phenylethyl)- is a chemical compound that is also known as methyldesorphine. It is a synthetic opioid analgesic drug that is structurally related to fentanyl. Methyldesorphine acts as a potent agonist at the μ-opioid receptor and has been found to have similar effects to morphine and fentanyl. Acetamide, N-methyl-N-(1-methyl-2-phenylethyl)- is commonly used in scientific research to understand the mechanisms of opioid receptor activation and for the development of new pain relieving medications. However, due to its potent and potentially addictive nature, it is a controlled substance and is not approved for medical use in humans.

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.

Cleavage reactions of the anorectic drug furfenorex

Unterhalt,Bause

, p. 878 - 878 (2007/10/03)

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