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882033-96-7

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882033-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 882033-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,0,3 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 882033-96:
(8*8)+(7*8)+(6*2)+(5*0)+(4*3)+(3*3)+(2*9)+(1*6)=177
177 % 10 = 7
So 882033-96-7 is a valid CAS Registry Number.

882033-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 3-fluoro-4-(methylsulfonyloxymethyl)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:882033-96-7 SDS

882033-96-7Downstream Products

882033-96-7Relevant articles and documents

QUINAZOLINONES AS PARP14 INHIBITORS

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Paragraph 1035; 1037, (2019/07/10)

The present invention relates to quinazolinones and related compounds which are inhibitors of PARP14 and are useful, for example, in the treatment of cancer and inflammatory diseases.

BICYCLIC AZAHETEROCYCLIC COMPOUNDS AS NR2B NMDA RECEPTOR ANTAGONISTS

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, (2016/07/05)

Disclosed are chemical entities of Formula (I): wherein R1 and Z are defined herein, as NR2B subtype selective receptor antagonists. Also disclosed are pharmaceutical compositions comprising a chemical entity of Formula (I), and methods of treating various diseases and disorders associated with NR2B antagonism, e.g., diseases and disorders of the CNS, such as depression, by administering a chemical entity of Formula (I).

Synthesis and SAR of substituted tetrahydrocarbazole derivatives as new NPY-1 antagonists

Di Fabio, Romano,Giovannini, Riccardo,Bertani, Barbara,Borriello, Manuela,Bozzoli, Andrea,Donati, Daniele,Falchi, Alessandro,Ghirlanda, Damiano,Leslie, Colin P.,Pecunioso, Angelo,Rumboldt, Giovanna,Spada, Simone

, p. 1749 - 1752 (2007/10/03)

The SAR of a new series of tetrahydrocarbazole derivatives is described: the appropriate decoration of this template led to the identification of a new class of NPY-1 antagonists showing good in vitro potency and a promising in vivo pharmacokinetic profil

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