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(R)-Norapocodeine is a chiral compound and the (R)-enantiomer of norapocodeine, an opioid analgesic derived from thebaine. It is a synthetically produced alkaloid with potential therapeutic applications, particularly in the management of pain. As an enantiomer, (R)-norapocodeine exhibits different biological activities compared to its (S)-counterpart, which can influence its efficacy and safety profile. The specific properties and pharmacological actions of (R)-norapocodeine are under investigation to better understand its role in medical treatments and to potentially develop new pain management strategies.

478-77-3

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478-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 478-77-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 478-77:
(5*4)+(4*7)+(3*8)+(2*7)+(1*7)=93
93 % 10 = 3
So 478-77-3 is a valid CAS Registry Number.

478-77-3SDS

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 (R)-Norapocodeine

1.2 Other means of identification

Product number -
Other names (6aR)-10-methoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-11-ol

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:478-77-3 SDS

478-77-3Downstream Products

478-77-3Relevant academic research and scientific papers

Aporphines. 27. Mechanistic Aspects of the Rearrangement of Thebaine and Codeine Analogues in Methanesulfonic Acid. Improved Method for Synthesis of N-Alkylated Aporphines

Granchelli, Felix E.,Filer, Crist N.,Soloway, Albert H.,Neumeyer, John L.

, p. 2275 - 2278 (2007/10/02)

The rearrangement of thebaine (1a), northebaine (1b), and N-(2-hydroxyethyl)northebaine (1c) in methanesulfonic acid leading to the formation of novel N-alkylated-2-O-methylated normorphothebaine derivatives 4a-c was investigated.We have observed that a s

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