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CAS

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21969-07-3

4-(4-nitrobenzyl)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 21969-07-3 Structure

  • Basic information

    1. Product Name: 4-(4-nitrobenzyl)phenol
    2. Synonyms:
    3. CAS NO:21969-07-3
    4. Molecular Formula: C13H11NO3
    5. Molecular Weight: 229.2313
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 21969-07-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 418.1°C at 760 mmHg
    3. Flash Point: 179.8°C
    4. Appearance: N/A
    5. Density: 1.279g/cm3
    6. Vapor Pressure: 1.39E-07mmHg at 25°C
    7. Refractive Index: 1.633
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-(4-nitrobenzyl)phenol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-(4-nitrobenzyl)phenol(21969-07-3)
    12. EPA Substance Registry System: 4-(4-nitrobenzyl)phenol(21969-07-3)

  • 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: 21969-07-3(Hazardous Substances Data)

21969-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21969-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,6 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 21969-07:
(7*2)+(6*1)+(5*9)+(4*6)+(3*9)+(2*0)+(1*7)=123
123 % 10 = 3
So 21969-07-3 is a valid CAS Registry Number.

21969-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(4-nitrophenyl)methyl]phenol

1.2 Other means of identification

Product number -
Other names 4-Nitro-4'-hydroxy-diphenylmethan

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:21969-07-3 SDS

21969-07-3Relevant articles and documents

Design, Synthesis, and Evaluation of Thyronamine Analogues as Novel Potent Mouse Trace Amine Associated Receptor 1 (m TAAR1) Agonists

Chiellini, Grazia,Nesi, Giulia,Digiacomo, Maria,Malvasi, Rossella,Espinoza, Stefano,Sabatini, Martina,Frascarelli, Sabina,Laurino, Annunziatina,Cichero, Elena,Macchia, Marco,Gainetdinov, Raul R.,Fossa, Paola,Raimondi, Laura,Zucchi, Riccardo,Rapposelli, Simona

, p. 5096 - 5107 (2015/07/02)

Trace amine associated receptor 1 (TAAR1) is a G protein coupled receptor (GPCR) expressed in brain and periphery activated by a wide spectrum of agonists that include, but are not limited to, trace amines (TAs), amphetamine-like psychostimulants, and end

SYNTHETIC ANALOGUES OF 3-IODOTHYRONAMINE (T1AM) AND USES THEREOF

-

, (2015/11/02)

Novel synthetic analogues of 3-iodothyronamine of formula (I), pharmaceutical compositions containing the same, and medical uses thereof are described.

4-NITROBENZYLATION OF PHENOL AND ANISOLE IN THE PRESENCE OF SMALL AMOUNTS OF FERRIC CHLORIDE

Tadzhimukhamedov, Kh. S.,Abdurasuleva, A. R.,Akhmedov, K. N.

, p. 944 - 946 (2007/10/02)

Unlike other substituted benzylchlorides, 4-nitrobenzyl chloride enters into reaction with phenol and anisole in the presence of 1E-2 - 1E-3 mole of ferric chloride.The yields of the 4-nitrobenzylphenols (anisoles) amount to 64-80percent.It was shown that

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