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3-(Allyloxy)aniline hydrochloride is an aminoalkyl ether and an aniline derivative, commonly used as a reagent in organic synthesis. It is known for its unique reactivity and versatility, forming stable complexes with various metal ions, making it a valuable tool in the field of organic chemistry. Its hydrochloride form is a white to off-white powder, often used as a catalyst in various chemical reactions and as a precursor to synthesize other organic compounds.

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  • 102879-28-7 Structure
  • Basic information

    1. Product Name: 3-(ALLYLOXY)ANILINE HYDROCHLORIDE
    2. Synonyms: 3-(ALLYLOXY)ANILINE HYDROCHLORIDE
    3. CAS NO:102879-28-7
    4. Molecular Formula: C9H11NO*ClH
    5. Molecular Weight: 185.65
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102879-28-7.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: 3-(ALLYLOXY)ANILINE HYDROCHLORIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(ALLYLOXY)ANILINE HYDROCHLORIDE(102879-28-7)
    11. EPA Substance Registry System: 3-(ALLYLOXY)ANILINE HYDROCHLORIDE(102879-28-7)
  • Safety Data

    1. Hazard Codes: Xi
    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: 102879-28-7(Hazardous Substances Data)

102879-28-7 Usage

Uses

Used in Organic Synthesis:
3-(Allyloxy)aniline hydrochloride is used as a reagent for its unique reactivity and versatility in organic synthesis, enabling the formation of various organic compounds.
Used in Coordination Chemistry:
3-(Allyloxy)aniline hydrochloride is used as a ligand for its ability to form stable complexes with various metal ions, making it useful in coordination chemistry and metal-based catalysis.
Used in Chemical Reactions as a Catalyst:
3-(Allyloxy)aniline hydrochloride is used as a catalyst in various chemical reactions due to its unique reactivity, enhancing the efficiency and selectivity of the reactions.
Used in the Synthesis of Other Organic Compounds:
3-(Allyloxy)aniline hydrochloride is used as a precursor in the synthesis of other organic compounds, contributing to the development of new chemical entities and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 102879-28-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,8,7 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 102879-28:
(8*1)+(7*0)+(6*2)+(5*8)+(4*7)+(3*9)+(2*2)+(1*8)=127
127 % 10 = 7
So 102879-28-7 is a valid CAS Registry Number.

102879-28-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-prop-2-enoxyaniline,hydrochloride

1.2 Other means of identification

Product number -
Other names 3-prop-2-enoxyaniline hydrochloride

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:102879-28-7 SDS

102879-28-7Upstream product

102879-28-7Relevant articles and documents

Design of postmetallocene catalytic systems of arylimine type for olefin polymerization: XIV.* synthesis of (N-allyloxyaryl)salicylaldimine ligands and their complexes with titanium(IV) dichloride

Oleinik,Oleinik,Ivanchev,Tolstikov

, p. 1071 - 1080 (2013/01/15)

By reaction of salicylaldehydes with bulky substituents in the positions 3 and 5 with o-, m-, and p-allyloxyaniline hydrochlorides in the presence of triethylamine a series of the corresponding (N-aryl)- salicylaldimines was obtained, which with TiCl2(OPr-i)2 afforded complexes of titanium(IV) dichloride L2TiCl2. Pleiades Publishing, Ltd., 2012.

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