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14357-78-9

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  • 6,14-Ethenomorphinan-7-methanol,17-(cyclopropylmethyl)-4,5-epoxy-18,19-dihydro-3-hydroxy-6-methoxy-a,a-dimethyl-, (5a,7a)-

    Cas No: 14357-78-9

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14357-78-9 Usage

Chemical Properties

Colourless or nearly colourless solid

Brand name

M50-50 Injection (Lemmon).

Biological Activity

Non-selective opioid receptor antagonist (K i values are 0.017, 0.072 and 0.23 nM for κ -, μ - and δ -opioid receptors).

Check Digit Verification of cas no

The CAS Registry Mumber 14357-78-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,5 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14357-78:
(7*1)+(6*4)+(5*3)+(4*5)+(3*7)+(2*7)+(1*8)=109
109 % 10 = 9
So 14357-78-9 is a valid CAS Registry Number.
InChI:InChI=1/C26H35NO4/c1-23(2,29)18-13-24-8-9-26(18,30-3)22-25(24)10-11-27(14-15-4-5-15)19(24)12-16-6-7-17(28)21(31-22)20(16)25/h6-7,15,18-19,22,28-29H,4-5,8-14H2,1-3H3/t18-,19-,22-,24-,25+,26-/m1/s1

14357-78-9SDS

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 Diprenorphine,17-(Cyclopropylmethyl)-4,5-epoxy-18,19-dihydro-3-hydroxy-6-methoxy-α,α-dimethyl-6,14-ethenomorphinan-7-methanol

1.2 Other means of identification

Product number -
Other names DIPRENORPHINE

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:14357-78-9 SDS

14357-78-9Related news

DIPRENORPHINE (cas 14357-78-9) as a stimulus in drug discrimination learning08/11/2019

Using the conditioned taste aversion baseline of drug discrimination learning, animals were trained to discriminate diprenorphine from distilled water. In subsequent generalization tests, the opiate antagonists naltrexone and naloxone and the mixed opiate agonist/antagonist nalorphine substitute...detailed

Morphine and DIPRENORPHINE (cas 14357-78-9) together potentiate intake of alcoholic beverages08/06/2019

Water-deprived rats were given a daily opportunity to take water or an ethanol solution. Prior to some opportunities to drink, some were injected with morphine (across procedures either 2.0, 7.5, or 20.0 mg/kg), diprenorphine (from 0.001 to 10.0 mg/kg), or a combination of diprenorphine and morp...detailed

14357-78-9Relevant articles and documents

PROCESS

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Page/Page column 14-15, (2019/06/11)

The present invention provides a process for the preparation of a compound of formula (2) : the process comprising reacting a compound of formula (1), a base and an alkylating agent R4-X in a nitrile-containing polar aprotic solvent to form the compound of formula (2), wherein the process is carried out at a temperature greater than 60 °C; and wherein R1, R2, R3, R4, and X are as defined in the specification.

Preparation of 6,14-Ethenomorphinane Derivatives

Marton, Janos,Szabo, Zoltan,Hosztafi, Sandor

, p. 915 - 920 (2007/10/02)

Buprenorphine (5j) and diprenorphine (5k) were synthesized from N-formyl-northebaine (1c) and N-benzyl-northebaine (1d) via new intermediates.N-cyclopropylmethyl-dihydronorthevinone 3d is a suitable compund for the synthesis of both 5j and 5k.We carried out detailed (1)H- and (13)C-NMR analysis of the new compounds. Key words: Buprenorphine; diprenorphine; rotamers, N-CHO; morphinane derivatives; alkaloids.

A procedure for preparing 3H-labeled tertiary amines. Synthesis of (3H)-6,14-endo-etheno-6,7,8,14-tetrahydrooripavine derivatives.

Lewis,Rance,Young

, p. 465 - 466 (2007/10/10)

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