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73674-86-9

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73674-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73674-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,7 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73674-86:
(7*7)+(6*3)+(5*6)+(4*7)+(3*4)+(2*8)+(1*6)=159
159 % 10 = 9
So 73674-86-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H25N3O3/c21-22-13-5-6-20(25)15-9-12-3-4-14(24)17-16(12)19(20,18(13)26-17)7-8-23(15)10-11-1-2-11/h3-4,11,15,18,24-25H,1-2,5-10,21H2/b22-13+/t15-,18+,19+,20-/m1/s1

73674-86-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R,4aS,7E,7aR,12bS)-3-(cyclopropylmethyl)-7-hydrazinylidene-2,4,5,6,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-4a,9-diol

1.2 Other means of identification

Product number -
Other names (5alpha)-17-(Cyclopropylmethyl)-4,5-epoxy-3,14-dihydroxymorphinan-6-one hydrazone

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:73674-86-9 SDS

73674-86-9Upstream product

73674-86-9Downstream Products

73674-86-9Relevant articles and documents

Long-Acting Opiate Agonists and Antagonists: 14-Hydroxydihydromorphinone Hydrazones

Pasternak, Gavril W.,Hahn, Elliot F.

, p. 674 - 676 (2007/10/02)

Two new long-acting hydrazone derivatives of 14-hydroxydihydromorphinones have been synthesized, oxymorphazone and naltrexazone.Both derivatives show high affinity for opiate binding sites in vitro, similar to naloxazone, the hydrazone analogue of naloxone.Sodium and manganese shifts imply that naltrexazone, like naloxazone, is a pure antagonist.By contrast, oxymorphazone inhibition of receptor binding is dramatically reduced by sodium and potentiated by manganese, suggesting it is an agonist.When given in vivo, all agents produce a significant inhibition of receptor binding for over 24 h despite extensive washing of the brain homogenates.Oxymorphone, naltrexone, and naloxone are without effect.Twenty-four hours after in vivo administration of oxymorphazone, 82percent of mice are still analgetic compared to only 17percent of oxymorphone-treated mice (p 0.005).Twenty-four hours after naltrexazone or naloxazone treatment all mice were protected from morphine analgesia (12 mg/kg; p 0.005), while naltrexone- and naloxone-treated animals did not differ significantly from saline-treated controls.

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