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143557-91-9

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143557-91-9 Usage

General Description

Tert-butyl 3-endo-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate is a synthetic compound with a complex chemical structure. It contains a tert-butyl group, a hydroxyl group, and a carboxylate group, as well as a bicyclic ring system with nitrogen. tert-butyl 3-endo-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate may be used in the development of pharmaceuticals or as a research tool in chemical and biological studies. Its unique structure gives it potential for specific interactions with biological systems, making it a valuable molecule for further exploration and potential applications in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 143557-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,5,5 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 143557-91:
(8*1)+(7*4)+(6*3)+(5*5)+(4*5)+(3*7)+(2*9)+(1*1)=139
139 % 10 = 9
So 143557-91-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H21NO3/c1-12(2,3)16-11(15)13-8-4-5-9(13)7-10(14)6-8/h8-10,14H,4-7H2,1-3H3

143557-91-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Boc-Nortropine

1.2 Other means of identification

Product number -
Other names tert-Butyl 3-endo-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate

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:143557-91-9 SDS

143557-91-9Relevant articles and documents

Bioorthogonal Self-Immolative Linker Based on Grob Fragmentation

Avenoza, Alberto,Bernardes, Gon?alo J. L.,Busto, Jesús H.,Corzana, Francisco,Ferhati, Xhenti,García-Sanmartín, Josune,Garrido, Pablo,Guerreiro, Ana,Jiménez-Moreno, Ester,Martínez, Alfredo,Peregrina, Jesús M.,Salas-Cubero, Marina

supporting information, p. 8580 - 8584 (2021/11/17)

A self-immolative bioorthogonal conditionally cleavable linker based on Grob fragmentation is described. It is derived from 1,3-aminocyclohexanols and allows the release of sulfonate-containing compounds in aqueous media. Modulation of the amine pKa promo

AZABENZIMIDAZOLE COMPOUNDS AND PHARMACEUTICAL

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Paragraph 0360, (2021/03/18)

The purpose of the present invention is to provide compounds having an M3 PAM action. Examples of the present invention include azabenzimidazole compounds represented, for example, by formula [I], and pharmacologically acceptable salts thereof. These comp

THERAPEUTICALLY ACTIVE BICYCLIC-SULPHONAMIDES AND PHARMACEUTICAL COMPOSITIONS

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Paragraph 0068, (2019/05/18)

Pharmaceutical compounds have a bicyclic-sulphonamide structure and pharmaceutical compositions including the compounds may be used in therapy as brain-cell-death protectants and may be used, for example, in the treatment of chronic neurodegenerative diseases. The compounds are active as inhibitors of N-acylethanolamine-hydrolysing acid amidase (NAAA) and may be used for the therapeutic treatment and prevention of pain and inflammatory disorders and other disorders which benefit from the modulation of fatty acid ethanolamides, particularly palmitoylethanolamide (PEA).

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