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CAS

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886362-19-2

3-(1'-AMINOETHYL)-1-N-BOC-ANILINE is a chemical compound characterized by the molecular formula C14H23N3O2. It is an aromatic amine that features a BOC-protected primary amine group and a terminal aminoethyl group. 3-(1'-AMINOETHYL)-1-N-BOC-ANILINE serves as a versatile building block in the synthesis of complex organic compounds due to its ability to undergo selective functionalization and participate in various chemical reactions, such as cross-coupling and reductive amination.

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  • Carbamic acid,N-[3-(1-aminoethyl)phenyl]-, 1,1-dimethylethyl ester Manufacturer/High quality/Best price/In stock

    Cas No: 886362-19-2

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  • 886362-19-2 Structure

  • Basic information

    1. Product Name: 3-(1'-AMINOETHYL)-1-N-BOC-ANILINE
    2. Synonyms: Carbamic acid, [3-(1-aminoethyl)phenyl]-, 1,1-dimethylethyl ester (9CI);tert-Butyl N-[3-(1-aminoethyl)phenyl]carbamate;1-(3-(BOC-AMINO)-PHENYL)-ETHYLAMINE
    3. CAS NO:886362-19-2
    4. Molecular Formula: C13H20N2O2
    5. Molecular Weight: 236.313
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 886362-19-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 303.6 °C at 760 mmHg
    3. Flash Point: 137.4 °C
    4. Appearance: /
    5. Density: 1.095 g/cm3
    6. Vapor Pressure: 0.000923mmHg at 25°C
    7. Refractive Index: 1.554
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-(1'-AMINOETHYL)-1-N-BOC-ANILINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(1'-AMINOETHYL)-1-N-BOC-ANILINE(886362-19-2)
    12. EPA Substance Registry System: 3-(1'-AMINOETHYL)-1-N-BOC-ANILINE(886362-19-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 886362-19-2(Hazardous Substances Data)

886362-19-2 Usage

Uses

Used in Pharmaceutical Industry:
3-(1'-AMINOETHYL)-1-N-BOC-ANILINE is used as a synthetic intermediate for the development of drug molecules. Its BOC-protected amine group allows for selective functionalization, which is crucial in the synthesis of pharmaceutical compounds with specific therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, 3-(1'-AMINOETHYL)-1-N-BOC-ANILINE is used as a precursor for the preparation of a wide range of chemical products. The presence of the aminoethyl group enables it to engage in various chemical reactions, contributing to the creation of diverse organic compounds for different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 886362-19-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,3,6 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 886362-19:
(8*8)+(7*8)+(6*6)+(5*3)+(4*6)+(3*2)+(2*1)+(1*9)=212
212 % 10 = 2
So 886362-19-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H20N2O2/c1-9(14)10-6-5-7-11(8-10)15-12(16)17-13(2,3)4/h5-9H,14H2,1-4H3,(H,15,16)

886362-19-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl N-[3-(1-aminoethyl)phenyl]carbamate

1.2 Other means of identification

Product number -
Other names (RS)-3-(1-aminoethyl)-N-(tert-butoxycarbonyl)phenylamine

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:886362-19-2 SDS

886362-19-2Downstream Products

886362-19-2Relevant articles and documents

A method for the selective protection of aromatic amines in the presence of aliphatic amines

Perron, Valerie,Abbott, Shaun,Moreau, Nancie,Lee, Devin,Penney, Christopher,Zacharie, Boulos

experimental part, p. 283 - 289 (2009/06/25)

A simple and efficient procedure has been developed for the regioselective protection of aromatic amines in the presence of aliphatic amines. The method is general for the preparation of mono-N-Boc, -N-Cbz, -N-Fmoc or -N-Alloc aromatic amines in high yield without affecting the aliphatic amines. This approach is applicable to substituted (aminoalkyl)aniline compounds with different functionalities and was employed to supply gram quantities of the protected aniline product. Georg Thieme Verlag Stuttgart · New York.

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