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871115-32-1

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871115-32-1 Usage

Description

TERT-BUTYL 4-AMINO-4-(AMINOMETHYL)PIPERIDINE-1-CARBOXYLATE is an organic compound that belongs to the class of piperidine carboxylates. It is a derivative of piperidine, a common building block in medicinal chemistry for the synthesis of pharmaceuticals and agrochemicals. TERT-BUTYL 4-AMINO-4-(AMINOMETHYL)PIPERIDINE-1-CARBOXYLATE features a tert-butyl group attached to the amino group of the piperidine ring, which enhances its stability and lipophilicity. The presence of the aminomethyl group adds versatility, making it a valuable precursor in the synthesis of bioactive compounds or as a ligand for metal catalysis. Its unique structural features lend potential to its applications in the development of new drugs and materials.

Uses

Used in Pharmaceutical Industry:
TERT-BUTYL 4-AMINO-4-(AMINOMETHYL)PIPERIDINE-1-CARBOXYLATE is used as a building block for the synthesis of various pharmaceuticals due to its enhanced stability and lipophilicity, which can improve the pharmacokinetic properties of the resulting drugs.
Used in Agrochemical Industry:
In the agrochemical industry, TERT-BUTYL 4-AMINO-4-(AMINOMETHYL)PIPERIDINE-1-CARBOXYLATE serves as a precursor for the development of new agrochemicals, leveraging its structural features to create compounds with potential pesticidal or herbicidal activities.
Used in Synthesis of Bioactive Compounds:
TERT-BUTYL 4-AMINO-4-(AMINOMETHYL)PIPERIDINE-1-CARBOXYLATE is used as a versatile precursor in the synthesis of bioactive compounds, taking advantage of its aminomethyl group to form diverse chemical entities with potential therapeutic or biological activity.
Used as a Ligand for Metal Catalysis:
In the field of catalysis, TERT-BUTYL 4-AMINO-4-(AMINOMETHYL)PIPERIDINE-1-CARBOXYLATE is utilized as a ligand for metal catalysts, contributing to the efficiency and selectivity of various chemical reactions, which can be beneficial in the synthesis of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 871115-32-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,1,1 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 871115-32:
(8*8)+(7*7)+(6*1)+(5*1)+(4*1)+(3*5)+(2*3)+(1*2)=151
151 % 10 = 1
So 871115-32-1 is a valid CAS Registry Number.

871115-32-1SDS

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 4-amino-4-(aminomethyl)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names TERT-BUTYL 4-AMINO-4-(AMINOMETHYL)PIPERIDINE-1-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:871115-32-1 SDS

871115-32-1Relevant articles and documents

Compositions for Treatment of Cystic Fibrosis and Other Chronic Diseases

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Paragraph 2519, (2015/09/22)

The present invention relates to pharmaceutical compositions comprising an inhibitor of epithelial sodium channel activity in combination with at least one ABC Transporter modulator compound of Formula A, Formula B, Formula C, or Formula D. The invention also relates to pharmaceutical formulations thereof, and to methods of using such compositions in the treatment of CFTR mediated diseases, particularly cystic fibrosis using the pharmaceutical combination compositions.

Organic Compounds

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Page/Page column 112, (2010/06/14)

A compound of Formula I in free or salt or solvate form, where R1, R2, R3, R4, R5, R6, R7, R8, R9, R10 and R11 have the meanings as indicated in the specification, is useful for treating diseases which respond to the blockade of the epithelial sodium channel. Pharmaceutical compositions that contain the compounds and processes for preparing the compounds are also described.

Spiro-rifamycin derivatives targeting RNA polymerase

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Page/Page column 14, (2008/06/13)

Compounds of the current invention relate to rifamycin derivatives having antimicrobial activities, including activities against drug-resistant microorganisms. More specifically, compounds of the current invention relate to a series of novel spiro rifamycin derivatives which have demonstrated potent antimicrobial activity.

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