Cas 42486-53-3,4-AMINO-2,6-DICHLOROPHENOL HYDROCHLORIDE

42486-53-3

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Basic information

Product Name: 4-AMINO-2,6-DICHLOROPHENOL HYDROCHLORIDE
Synonyms: 4-amino-2,6-dichloro-phenohydrochloride;TIMTEC-BB SBB003405;4-AMINO-2,6-DICHLOROPHENOL HCL;4-AMINO-2,6-DICHLOROPHENOL HYDROCHLORIDE;4-AMINO-2,6-DICHLOROPHENOL HYDROCHLORIDE 99%;4-Amino-2,6-dichlorophenol hydrochloride,99%
CAS NO:42486-53-3
Molecular Formula: C₆H₅Cl₂NO*ClH
Molecular Weight: 214.48
EINECS: 255-846-5
Product Categories: N/A
Mol File: 42486-53-3.mol

Chemical Properties

Melting Point: 280-285 °C
Boiling Point: 303.6°Cat760mmHg
Flash Point: 137.4°C
Appearance: /
Density: 1.56g/cm³
Vapor Pressure: 0.000511mmHg at 25°C
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-AMINO-2,6-DICHLOROPHENOL HYDROCHLORIDE(CAS DataBase Reference)
NIST Chemistry Reference: 4-AMINO-2,6-DICHLOROPHENOL HYDROCHLORIDE(42486-53-3)
EPA Substance Registry System: 4-AMINO-2,6-DICHLOROPHENOL HYDROCHLORIDE(42486-53-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: 24/25
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 42486-53-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 42486-53-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,4,8 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 42486-53:
(7*4)+(6*2)+(5*4)+(4*8)+(3*6)+(2*5)+(1*3)=123
123 % 10 = 3
So 42486-53-3 is a valid CAS Registry Number.

InChI:InChI=1/C6H5Cl2NO.ClH/c7-4-1-3(9)2-5(8)6(4)10;/h1-2,10H,9H2;1H

42486-53-3Upstream product

146901-66-8 2,6-dichloro-4-phenylazo-phenol

42486-53-3Downstream Products

500-85-6 indophenol

42486-53-3Relevant academic research and scientific papers

A simple reduction method of azo-compounds to amines using Fe powder in the presence of NH4Cl

Mobinikhaledi, Akbar,Foroughifar, Naser,Jirandehi, Hasan Fathinejad

, p. 755 - 757 (2007)

A series of azo-compounds were reduced to related aromatic amines in the presence of Fe powder and ammonium chloride. This one step protocol led to the formation of products in middle to high yields, especially when electron releasing substituted aromatic azo-compounds were reduced.

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