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205999-74-2

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205999-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 205999-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,9,9 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 205999-74:
(8*2)+(7*0)+(6*5)+(5*9)+(4*9)+(3*9)+(2*7)+(1*4)=172
172 % 10 = 2
So 205999-74-2 is a valid CAS Registry Number.

205999-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4(R)-(3-hydroxyphenyl)-3(R),4-dimethyl-1-tert-butyloxycarbonylpiperidine

1.2 Other means of identification

Product number -
Other names (3R,4R)-4-(3-Hydroxy-phenyl)-3,4-dimethyl-piperidine-1-carboxylic acid tert-butyl ester

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:205999-74-2 SDS

205999-74-2Downstream Products

205999-74-2Relevant articles and documents

NOVEL OPIOID ANTAGONISTS

-

Page/Page column 30; 47-48, (2008/06/13)

Certain quinolizidine and octahydropyridopyrazine compounds, pharmaceutical compositions, and methods of their use, inter alia, as opioid receptor antagonists are disclosed.

trans-3,4-Dimethyl-4-(3-carboxamidophenyl)piperidines: A novel class of μ-Selective opioid antagonists

Le Bourdonnec, Bertrand,Belanger, Serge,Cassel, Joel A.,Stabley, Gabriel J.,DeHaven, Robert N.,Dolle, Roland E.

, p. 4459 - 4462 (2007/10/03)

trans-3,4-Dimethyl-4-(3-carboxamidophenyl)piperidines constitute a novel class of μ opioid receptor antagonists. The CONH2 group was found to be an effective isostere of the phenolic OH moiety. Structure-activity relationships at the piperidine

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