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Tert-butyl octahydropyrrolo[3.4-b]pyridine-1-carboxylate is a complex carboxylate ester chemical compound, derived from the combination of tert-butyl, octahydropyrrolo, and pyridine-1-carboxylate moieties. Its intricate molecular structure suggests potential pharmacological activity and presents opportunities for the development of new synthetic methods and strategies in both medicinal and organic chemistry.

159991-07-8

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159991-07-8 Usage

Uses

Used in Medicinal Chemistry:
Tert-butyl octahydropyrrolo[3.4-b]pyridine-1-carboxylate is used as a potential pharmaceutical candidate for the development of new drugs due to its unique molecular structure and possible pharmacological activity.
Used in Organic Chemistry Research:
In the field of organic chemistry, tert-butyl octahydropyrrolo[3.4-b]pyridine-1-carboxylate serves as a subject of interest for the exploration of new synthetic methods and strategies, given its distinctive molecular composition.
However, it is important to note that further research is required to fully understand the properties and potential uses of tert-butyl octahydropyrrolo[3.4-b]pyridine-1-carboxylate in various applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 159991-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,9,9 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 159991-07:
(8*1)+(7*5)+(6*9)+(5*9)+(4*9)+(3*1)+(2*0)+(1*7)=188
188 % 10 = 8
So 159991-07-8 is a valid CAS Registry Number.

159991-07-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl (4aS,7aS)-2,3,4,4a,5,6,7,7a-octahydropyrrolo[3,4-b]pyridine-1-carboxylate

1.2 Other means of identification

Product number -
Other names (S,S)-2-tert-butoxycarbonyl-2,8-diazabicyclo[4.3.0]nonan

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:159991-07-8 SDS

159991-07-8Downstream Products

159991-07-8Relevant academic research and scientific papers

LACTAM ACETAMIDES AS CALCIUM CHANNEL BLOCKERS

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Page/Page column 18, (2011/10/10)

The present application relates to calcium channel inhibitors containing compounds of formula (I) wherein Ar1, n, R1, X and Y are as defined in the specification. The present application also relates to compositions comprising such compounds, and methods of treating conditions and disorders using such compounds and compositions.

NOVEL COMPOUNDS AS CALCIUM CHANNEL BLOCKERS

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Page/Page column 88, (2010/04/27)

The present application relates to calcium channel inhibitors containing compounds of formula (I) wherein Ar1, Ar2, L1, L2, n, R1, R4, X and Y are as defined in the specification. The present application also relates to compositions comprising such compounds, and methods of treating conditions and disorders using such compounds and compositions.

QUINOLONECARBOXYLIC ACID COMPOUNDS, PREPARATION METHODS AND PHARMACEUTICAL USES THEREOF

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Page/Page column 10, (2010/11/26)

This invention discloses novel quinolonecarboxylic acid derivatives, pharmaceutically acceptable salts or hydrates thereof, and their preparation methods and medical uses. The compounds in this invention show potent antibacterial activity against broad-sp

Bicyclic amine derivatives

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, (2008/06/13)

A compound represented by formula (I) or a salt thereof: STR1 wherein X1 and X2 each represent a halogen atom; R1 represents a hydrogen atom or a substituent; R2 represents a substituted or unsubstituted bicyclic heterocyclic substituent of the following formula; STR2 wherein R3, R4, Y, Z, m, n, p, q and r are as defined herein; A represents a nitrogen atom or a substituted carbon atom; and R represents a hydrogen atom or a substituent. The compound exhibits potent antimicrobial activity and also high safety due to reduced lipophilicity.

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