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4-amino-2-(prop-2-en-1-yl)phenol, an aromatic amine with the molecular formula C9H11NO, features a hydroxyl group and an alkyl group attached to its benzene ring. This versatile compound is characterized by its unique structure and properties, making it suitable for a range of chemical reactions and synthesis processes.

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  • 35736-25-5 Structure
  • Basic information

    1. Product Name: 4-amino-2-(prop-2-en-1-yl)phenol
    2. Synonyms:
    3. CAS NO:35736-25-5
    4. Molecular Formula: C9H11NO
    5. Molecular Weight: 149.1897
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 35736-25-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 302.4°C at 760 mmHg
    3. Flash Point: 136.7°C
    4. Appearance: N/A
    5. Density: 1.108g/cm3
    6. Vapor Pressure: 0.000554mmHg at 25°C
    7. Refractive Index: 1.603
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-amino-2-(prop-2-en-1-yl)phenol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-amino-2-(prop-2-en-1-yl)phenol(35736-25-5)
    12. EPA Substance Registry System: 4-amino-2-(prop-2-en-1-yl)phenol(35736-25-5)
  • 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: 35736-25-5(Hazardous Substances Data)

35736-25-5 Usage

Uses

Used in Dye and Pigment Production:
4-amino-2-(prop-2-en-1-yl)phenol is utilized as a key intermediate in the synthesis of dyes and pigments, contributing to the coloration and stability of these products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 4-amino-2-(prop-2-en-1-yl)phenol serves as a building block for the development of various drugs, capitalizing on its reactivity and functional groups to create medicinal compounds.
Used in Organic Chemistry Research:
4-amino-2-(prop-2-en-1-yl)phenol is employed as a research compound in organic chemistry, where its unique structure allows for the exploration of new reactions and the synthesis of novel organic molecules.
Used in Biochemical Research:
Due to its potential interactions with biological systems, 4-amino-2-(prop-2-en-1-yl)phenol is also used in biochemical research to study its effects and possible applications in biological processes.
Safety Note:
It is crucial to handle 4-amino-2-(prop-2-en-1-yl)phenol with care, as it may present health hazards if mismanaged or improperly disposed of. Proper safety measures should be taken during its use to mitigate any risks.

Check Digit Verification of cas no

The CAS Registry Mumber 35736-25-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,7,3 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 35736-25:
(7*3)+(6*5)+(5*7)+(4*3)+(3*6)+(2*2)+(1*5)=125
125 % 10 = 5
So 35736-25-5 is a valid CAS Registry Number.

35736-25-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-2-prop-2-enylphenol

1.2 Other means of identification

Product number -
Other names 2-allyl-4-amino-phenol

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:35736-25-5 SDS

35736-25-5Relevant articles and documents

Aluminium chloride-potassium iodide-acetonitrile system: A mild reagent system for aromatic claisen rearrangement at ambient temperature

Bhattacharyya, Nayan Kamal,Dutta, Deepjyoti,Biswas, Joydeep

, (2021/06/28)

Claisen rearrangement is used as the standard methods for the generation of complex organic substance. It is one of the well-known methods for the introduction of carbon-carbon bond. We have developed a protocol using allyl aryl ether as a substrate and AlCl3-KI as a mild reagent system and acetonitrile (CH3CN) is taken as solvent at ambient temperature. The reagent system presented in this current work is found to be appropriate for Claisen rearrangement of several aromatic alcohols with excellent yields.

Hair conditioning compositions and their use in hair colouring compositions

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, (2008/06/13)

The present invention relates to a hair care composition comprising a aminofunctional polysiloxane having a specified average effective particle size which provides improved durable conditioning particularly when utilised in conjunction with a hair colouring composition.

Hair colouring and conditioning compositions

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, (2008/06/13)

A hair colouring and conditioning composition comprising: (a) a hair colouring agent; and (b) a hair conditioning agent; wherein the composition provides an Average Combing Index Value of greater than 1.2 as measured by the Combing Technical Test Method. The products can provide excellent hair colouring together with excellent conditioning, reduced hair damage, brittleness and dryness, and is convenient and easy to use.

HAIR COLORING COMPOSITIONS

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, (2008/06/13)

A hair coloring composition comprising: (a) from about 0.0003 moles (per 100 g of composition) to less than about 0.09 moles (per 100 g of composition) of an inorganic peroxygen oxidizing agent; and (b) an oxidative hair coloring agent; wherein the pH of each of (a) and (b) is in the range of from about 1 to about 6 and wherein the combined mixture of (a) and (b) has a pH in the range of from about 1 to about 6. The products can provide excellent hair coloring and in-use efficacy benefits including excellent initial color and good wash fastness in combination with reduced hair damage at low pH.

HAIR COLORING COMPOSITIONS

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A hair coloring composition comprising: (a) a preformed organic peroxyacid oxidising agent; and (b) an oxidative hair coloring agent; wherein the pH of each of components (a) and (b) is in the range of from about pH 1 to less than about pH 7 and wherein the pH of the composition is in the range of from about pH 1 to less than about pH 7. The products can provide excellent hair coloring and in-use efficacy benefits including excellent initial color and good wash fastness in combination with reduced hair damage at low pH.

Enzyme-activated oxidative process for coloring hair

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An enzyme-based oxidative process for coloring hair wherein the hair is exposed to a solution having a pH of about 4 to about 10 and containing hydrogen peroxide, soybean peroxidase enzyme and one or more oxidation dye precursors.

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