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103587-51-5

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103587-51-5 Usage

Description

O-(tert-butyldiphenylsilyl)hydroxylamine is an organic compound that serves as a crucial intermediate in the synthesis of various pharmaceutical compounds. It is characterized by its unique structure, which includes a tert-butyldiphenylsilyl group attached to a hydroxylamine moiety. This structure endows it with specific reactivity and properties that make it valuable in the development of certain medications.

Uses

Used in Pharmaceutical Synthesis:
O-(tert-butyldiphenylsilyl)hydroxylamine is used as an intermediate in the synthesis of N-Hydroxy Vortioxetine O-β-D-Glucuronide Sodium Salt (H996005). O-(tert-butyldiphenylsilyl)hydroxylamine is a metabolite of Vortioxetine (V766000, HBr), a multimodal serotonergic agent with a wide range of applications in the treatment of various conditions related to the serotonin system.
In the pharmaceutical industry, O-(tert-butyldiphenylsilyl)hydroxylamine plays a vital role in the development of Vortioxetine and its derivatives. Vortioxetine is known for its ability to inhibit multiple serotonin receptors, including 5-HT1A, 5-HT1B, 5-HT3A, and 5-HT7, as well as the serotonin transporter (SERT). This unique profile makes Vortioxetine a promising candidate for the treatment of various psychiatric and neurological disorders, such as depression, anxiety, and obsessive-compulsive disorder.
The use of O-(tert-butyldiphenylsilyl)hydroxylamine in the synthesis of Vortioxetine and its metabolites highlights its importance in the development of novel therapeutic agents with potential applications in the treatment of a wide range of conditions. Its unique structural features and reactivity make it a valuable component in the design and synthesis of new drugs targeting the serotonin system.

Check Digit Verification of cas no

The CAS Registry Mumber 103587-51-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,5,8 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 103587-51:
(8*1)+(7*0)+(6*3)+(5*5)+(4*8)+(3*7)+(2*5)+(1*1)=115
115 % 10 = 5
So 103587-51-5 is a valid CAS Registry Number.

103587-51-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name O-(tert-Butyldiphenylsilyl)hydroxylamine

1.2 Other means of identification

Product number -
Other names O-[tert-butyl(diphenyl)silyl]hydroxylamine

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:103587-51-5 SDS

103587-51-5Relevant articles and documents

Ferrier sulfamidoglycosylation of glycals catalyzed by nitrosonium tetrafluoroborate: Towards new carbonic anhydrase glycoinhibitors

Ombouma, Joanna,Vullo, Daniela,Supuran, Claudiu T.,Winum, Jean-Yves

, p. 6353 - 6359 (2014)

Ferrier sulfamidoglycosylation of glycals catalyzed by nitrosonium tetrafluoroborate allowed the preparation of hydroxysulfamide glycosides in good yields with a good α stereoselectivity. A variety of mono-saccharide derivatives was synthesized using this

Thiyl radical-mediated cyclization of ω-alkynyl O-tert-butyldiphenylsilyloximes

Shibata, Nina,Tsuchiya, Takahisa,Hashimoto, Yoshimitsu,Morita, Nobuyoshi,Ban, Shintaro,Tamura, Osamu

supporting information, p. 3025 - 3034 (2017/04/10)

ω-Alkynyl O-tert-butyldiphenylsilyloximes, upon treatment with odorless 4-tert-butylbenzenethiol in the presence of azobisisobutyronitrile (AIBN) in refluxing benzene, underwent addition of a thiyl radical to the alkynyl group followed by radical cyclizat

METABOLITES OF PRINOMASTAT AND THEIR SYTHESIS

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Page 22, (2010/02/04)

Metabolites of a matrix metalloproteinase inhibitor prinomastat their synthesis composition, and method of using same. These metabolites are: (3S)-N-hydroxy-4-(4-((1-oxy-pyrid-4-yl)oxy)benzenesulfonyl)-2,2-dimethyl-tetrahydro-2H-1,4-thiazine-3-carboxamide

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