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Thiocyanic acid, 2-amino-1-naphthalenyl ester, also known as 2-amino-1-naphthalenyl thiocyanate, is an organic compound with the chemical formula C11H8N2S. It is derived from thiocyanic acid, which is a simple organic compound consisting of a hydrogen atom, a cyanide group, and a sulfur atom. The 2-amino-1-naphthalenyl ester is formed by the esterification of thiocyanic acid with 2-amino-1-naphthol, resulting in a yellow crystalline solid. Thiocyanic acid, 2-amino-1-naphthalenyl ester is primarily used as a chemical intermediate in the synthesis of various dyes, pigments, and pharmaceuticals. It is also known for its potential applications in analytical chemistry as a reagent for the detection of metal ions. Due to its reactivity and potential health hazards, it is important to handle Thiocyanic acid, 2-amino-1-naphthalenyl ester with care, following proper safety protocols.

2476-69-9

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2476-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2476-69-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,7 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2476-69:
(6*2)+(5*4)+(4*7)+(3*6)+(2*6)+(1*9)=99
99 % 10 = 9
So 2476-69-9 is a valid CAS Registry Number.

2476-69-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-aminonaphthalen-1-yl) thiocyanate

1.2 Other means of identification

Product number -
Other names (2-Amino-naphthyl-(1))-rhodanid

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:2476-69-9 SDS

2476-69-9Relevant academic research and scientific papers

1-Methyl-3-phenyl-3-thiocyanato-1H,3H-quinoline-2,4-dione: A Novel Thiocyanating Agent

Klasek, Antonin,Mrkvicka, Vladimir

, p. 747 - 752 (2003)

Under mild reaction conditions, the thiocyanato group is selectively transferred from 1-methyl-3-phenyl-3-thiocyanato-1H,3H-quinoline-2,4-dione (3) to some nucleophiles. Aliphatic primary and secondary amines are converted to S-cyanothiohydroxylamines, anilines afford p-thiocyanatoanilines, Wittig reagent is thiocyanated in α-position, and thiols are oxidized to disulfides.

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