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Tert-butyl 3-(aminomethyl)-3-fluoropiperidine-1-carboxylate is a chemical compound with a molecular formula C13H23FN2O2. It is a derivative of piperidine, a naturally occurring heterocyclic amine that is commonly found in plants and animals. tert-butyl 3-(aMinoMethyl)-3-fluoropiperidine-1-carboxylate is a white solid that is soluble in organic solvents and has a molecular weight of 250.33 g/mol. The presence of the tert-butyl group at the nitrogen atom provides steric hindrance, which can influence the reactivity and properties of the compound in various chemical reactions.

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  • 1209781-11-2 Structure
  • Basic information

    1. Product Name: tert-butyl 3-(aMinoMethyl)-3-fluoropiperidine-1-carboxylate
    2. Synonyms: tert-butyl 3-(aMinoMethyl)-3-fluoropiperidine-1-carboxylate;3-FLUORO-3-HYDROXYMETHYL-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER;1-Boc-3-fluoropiperidine-3-Methanol;tert-Butyl 3-fluoro-3-(hydroxymethyl)piperidine-1-carboxylate
    3. CAS NO:1209781-11-2
    4. Molecular Formula: C11H21FN2O2
    5. Molecular Weight: 232.2950432
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1209781-11-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: tert-butyl 3-(aMinoMethyl)-3-fluoropiperidine-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl 3-(aMinoMethyl)-3-fluoropiperidine-1-carboxylate(1209781-11-2)
    11. EPA Substance Registry System: tert-butyl 3-(aMinoMethyl)-3-fluoropiperidine-1-carboxylate(1209781-11-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1209781-11-2(Hazardous Substances Data)

1209781-11-2 Usage

Uses

Used in Pharmaceutical Industry:
Tert-butyl 3-(aminomethyl)-3-fluoropiperidine-1-carboxylate is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure and properties make it a valuable building block for the development of new drugs, particularly in the areas of central nervous system disorders and pain management.
Used in Chemical Research:
In the field of chemical research, tert-butyl 3-(aminomethyl)-3-fluoropiperidine-1-carboxylate serves as a versatile compound for studying various chemical reactions and mechanisms. The steric hindrance provided by the tert-butyl group allows researchers to explore its effects on reaction rates, selectivity, and product formation, contributing to a deeper understanding of organic chemistry principles.
Used in Drug Development:
Tert-butyl 3-(aminomethyl)-3-fluoropiperidine-1-carboxylate is used as a key component in the development of new drugs, particularly for the treatment of neurological disorders and pain conditions. Its unique structure and properties enable the design of novel drug candidates with improved efficacy, selectivity, and safety profiles.
Used in Organic Synthesis:
As a white solid that is soluble in organic solvents, tert-butyl 3-(aminomethyl)-3-fluoropiperidine-1-carboxylate is utilized in various organic synthesis processes. Its reactivity and properties make it a suitable candidate for the preparation of a wide range of organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 1209781-11-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,9,7,8 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1209781-11:
(9*1)+(8*2)+(7*0)+(6*9)+(5*7)+(4*8)+(3*1)+(2*1)+(1*1)=152
152 % 10 = 2
So 1209781-11-2 is a valid CAS Registry Number.

1209781-11-2SDS

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-3-(hydroxymethyl)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-BOC-3-FLUOROPIPERIDINE-3-METHANOL

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:1209781-11-2 SDS

1209781-11-2Relevant articles and documents

PYRIDYL DERIVATIVES AS BROMODOMAIN INHIBITORS

-

, (2017/11/04)

The present invention relates to compounds of formula (I) and salts thereof, pharmaceutical compositions containing such compounds and to their use in therapy.

BENZO[B]FURANS AS BROMODOMAIN INHIBITORS

-

, (2017/11/06)

The present invention relates to compounds of formula (I) and salts thereof, pharmaceutical compositions containing such compounds and to their use in therapy.

1,3-THIAZOL-2-YL SUBSTITUTED BENZAMIDES

-

Page/Page column 341; 342, (2016/07/05)

The present invention relates to 1,3-thiazol-2-yl substituted benzamide compounds of general formula (I) as described and defined herein, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of neurogenic disorder, as a sole agent or in combination with other active ingredients.

Asymmetric Fluorination Approach to the Scalable Synthesis of a SYK Inhibitor

Curtis, Neil R.,Davies, Suzanne H.,Gray, Matthew,Leach, Stuart G.,McKie, Ross A.,Vernon, Lois E.,Walkington, Andrew J.

, p. 865 - 871 (2015/07/27)

A large-scale process for the synthesis of SYK inhibitor 1 has been developed and used to deliver multi-kilogram yields of this active pharmaceutical ingredient. Integral to the scalable process is a combined chiral auxiliary and chiral catalyst mediated

PYRIDO[3,4-B]PYRAZINE DERIVATIVES AS SYK INHIBITORS

-

, (2014/02/15)

A compound of formula (I): or a salt thereof; which is an inhibitor of spleen tyrosine kinase (Syk) and therefore potentially of use in treating diseases resulting from inappropriate activation of mast cells, macrophages, and B-cells and related inflammatory responses and tissue damage, for instance inflammatory disease and/or allergic disorders, and in cancer therapy, specifically heme malignancies, and autoimmune conditions.

7-(lH-PYRAZOL-4-YL)-1,6-NAPHTHYRIDINE COMPOUNDS AS SYK INHIBITORS

-

Paragraph 0457-0458, (2013/03/26)

The present invention relates to a compound of formula (I): or a salt thereof; which is an inhibitor of spleen tyrosine kinase (Syk) and therefore potentially of use in treating diseases resulting from inappropriate activation of mast and/or basophil cells, macrophages, and B-cells and related inflammatory responses and tissue damage, for instance inflammatory disease and/or allergic disorders, and in cancer therapy, specifically heme malignancies, chronic spontaneous urticaria and autoimmune conditions.

PYRIDO[3,4-B]PYRAZINE DERIVATIVES AS SYK INHIBITORS

-

, (2012/10/07)

A compound of formula (I) or a salt thereof; which is an inhibitor of spleen tyrosine kinase (Syk) and therefore potentially of use in treating diseases resulting from inappropriate activation of mast cells, macrophages, and B-cells and related inflammatory responses and tissue damage, for instance inflammatory disease and/or allergic disorders, and in cancer therapy, specifically heme malignancies, and autoimmune conditions.

7-(1H-PYRAZOL-4-YL)-1,6-NAPHTHYRIDINE COMPOUNDS AS SYK INHIBITORS

-

, (2011/11/13)

A compound of formula (I) or a salt thereof; which is an inhibitor of spleen tyrosine kinase (Syk) and therefore potentially of use in treating diseases resulting from inappropriate activation of mast and/or basophil cells, macrophages, and B-cells and related inflammatory responses and tissue damage, for instance inflammatory disease and/or allergic disorders, and in cancer therapy, specifically heme malignancies, chronic spontaneous urticaria and autoimmune conditions.

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