Cas 3372-02-9,NORMORPHINE HYDROCHLORIDE METHANOL*SOLUT ION 100 MIC

3372-02-9

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Basic information

Product Name: NORMORPHINE HYDROCHLORIDE METHANOL*SOLUT ION 100 MIC
Synonyms: NORMORPHINE HYDROCHLORIDE METHANOL*SOLUT ION 100 MIC;normorphine hydrochloride*monohydrate--dea schedu;(5alpha,6alpha)-7,8-didehydro-4,5-epoxymorphinan-3,6-diol hydrochloride;Normorphine hydrochloride;Normorphine hydrochloride monohydrate ;HQNHDHNPDOTERW-VIGPQYPBSA-N
CAS NO:3372-02-9
Molecular Formula: C₁₆H₁₇NO₃*ClH
Molecular Weight: 325.79
EINECS: 222-152-9
Product Categories: N/A
Mol File: 3372-02-9.mol
Article Data: 2

Chemical Properties

Melting Point: N/A
Boiling Point: 485.8°C at 760 mmHg
Flash Point: 247.6°C
Appearance: /
Density: 1.48g/cm³
Vapor Pressure: 2.99E-10mmHg at 25°C
Refractive Index: 1.733
Storage Temp.: ?20°C
Solubility: N/A
CAS DataBase Reference: NORMORPHINE HYDROCHLORIDE METHANOL*SOLUT ION 100 MIC(CAS DataBase Reference)
NIST Chemistry Reference: NORMORPHINE HYDROCHLORIDE METHANOL*SOLUT ION 100 MIC(3372-02-9)
EPA Substance Registry System: NORMORPHINE HYDROCHLORIDE METHANOL*SOLUT ION 100 MIC(3372-02-9)

Safety Data

Hazard Codes: Xn,T,F
Statements: 22-39/23/24/25-23/24/25-11
Safety Statements: 36/37/39-45-36/37-16-7
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 3372-02-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 3372-02-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,7 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3372-02:
(6*3)+(5*3)+(4*7)+(3*2)+(2*0)+(1*2)=69
69 % 10 = 9
So 3372-02-9 is a valid CAS Registry Number.

InChI:InChI=1/C16H17NO3/c18-11-3-1-8-7-10-9-2-4-12(19)15-16(9,5-6-17-10)13(8)14(11)20-15/h1-4,9-10,12,15,17-19H,5-7H2/t9?,10-,12+,15+,16+/m1/s1

3372-02-9Upstream product

3372-02-9Downstream Products

466-97-7 normorphine

3372-02-9Relevant articles and documents

Efficient iron-catalyzed n-demethylation of tertiary amine-N-oxides under oxidative conditions

Kok, Gaik B.,Scammells, Peter J.

, p. 1515 - 1521 (2012/02/04)

An investigation into the influence of oxidative conditions on the efficiency of opiate N-demethylation using iron powder has been carried out under non-classical Polonovski conditions. This approach involves a two-step process of N-oxidation and subsequent treatment of the intermediate N-oxide hydrochloride with the redox catalyst. Significant improvements in rate and yield have been realized for these reactions in the presence of molecular oxygen. In this context, further rate enhancement was achieved by the judicious addition of small amounts of ferric ions, leading to a concomitant reduction in the amount of the zero-valent iron primary catalyst that is required. This has led to a generalized improved methodology for the N-demethylation of oripavine, codeine, morphine, and thebaine. This protocol can also be carried out in one-pot without the need to isolate the intermediate N-oxide.