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63515-89-9

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63515-89-9 Usage

Chemical class

Piperidinone derivatives

Appearance

White crystalline powder

Molecular weight

259.34 g/mol

Primary use

Intermediate in the synthesis of pharmaceuticals and research chemicals

Specific applications

Production of opioid agonists and antagonists

Recreational use

Potential for opioid-like effects

Legal status

Controlled substance in many countries

Regulation

Use and distribution are strictly regulated due to psychoactive properties and potential for abuse.

Check Digit Verification of cas no

The CAS Registry Mumber 63515-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,1 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63515-89:
(7*6)+(6*3)+(5*5)+(4*1)+(3*5)+(2*8)+(1*9)=129
129 % 10 = 9
So 63515-89-9 is a valid CAS Registry Number.

63515-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-4-ethyl-4-methylpiperidine-2,6-dione

1.2 Other means of identification

Product number -
Other names N-Benzyl-3-ethyl-3-methylglutarimid

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:63515-89-9 SDS

63515-89-9Downstream Products

63515-89-9Relevant articles and documents

Chemoselective hydrogenation of imides catalyzed by Cp*Ru(PN) complexes and its application to the asymmetric synthesis of paroxetine

Ito, Masato,Sakaguchi, Ayaka,Kobayashi, Chika,Ikariya, Takao

, p. 290 - 291 (2008/04/18)

This work represents the first catalytic hydrogenation of imides into amides and primary alcohols, in which the unique chemoselectivity is originated from the bifunctional nature of ruthenium-NH moiety in the catalyst. Copyright

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