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O-Isobutyryl Naltrexone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

861238-38-2

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861238-38-2 Usage

Chemical Properties

White Solid

Uses

Naltrexone (N285750) derivative.

Check Digit Verification of cas no

The CAS Registry Mumber 861238-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,1,2,3 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 861238-38:
(8*8)+(7*6)+(6*1)+(5*2)+(4*3)+(3*8)+(2*3)+(1*8)=172
172 % 10 = 2
So 861238-38-2 is a valid CAS Registry Number.

861238-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names (5|A)-17-(Cyclopropylmethyl)-4,5-epoxy-14-hydroxy-3-(2-methyl-1-oxopropoxy)-morphinan-6-one

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:861238-38-2 SDS

861238-38-2Downstream Products

861238-38-2Relevant academic research and scientific papers

Human skin permeation of branched-chain 3-O-alkyl ester and carbonate prodrugs of naltrexone

Vaddi, Haranath K.,Hamad, Mohamed O.,Chen, Jianhong,Banks, Stan L.,Crooks, Peter A.,Stinchcomb, Audra L.

, p. 758 - 765 (2005)

Purpose. Physicochemical characterization and in vitro human skin diffusion studies of branched-chain ester and carbonate prodrugs of naltrexone (NTX) were compared and contrasted with straight-chain ester and carbonate NTX prodrugs. Methods. Human skin p

SYNTHESIS OF (R)-N-METHYLNALTREXONE

-

Page/Page column 57-58; 4/6, (2010/11/25)

This invention relates to stereoselective synthesis of R-MNTX and intermediates thereof, pharmaceutical preparations comprising R-MNTX or intermediates thereof and methods for their use.

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