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115044-52-5

115044-52-5

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115044-52-5 Usage

Chemical Properties

Yellow Solid

Uses

3-Nitroaniline acts as an azo dye used in analytical toxicity studies. 3-Nitroaniline-2,4,5,6-d4 is the labeled version.

Check Digit Verification of cas no

The CAS Registry Mumber 115044-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,0,4 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 115044-52:
(8*1)+(7*1)+(6*5)+(5*0)+(4*4)+(3*4)+(2*5)+(1*2)=85
85 % 10 = 5
So 115044-52-5 is a valid CAS Registry Number.

115044-52-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-NITROANILINE-2,4,5,6-D4

1.2 Other means of identification

Product number -
Other names -

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:115044-52-5 SDS

115044-52-5Upstream product

115044-52-5Downstream Products

115044-52-5Relevant articles and documents

Hydrogen-deuterium exchange of aromatic amines and amides using deuterated trifluoroacetic acid

Giles, Richard,Lee, Amy,Jung, Erica,Kang, Aaron,Jung, Kyung Woon

, p. 747 - 749 (2015)

The H-D exchange of aromatic amines and amides, including pharmaceutically relevant compounds such as acetaminophen and diclofenac, was investigated using CF3COOD as both the sole reaction solvent and source of deuterium label. The described method is amenable to efficient deuterium incorporation for a wide variety of substrates possessing both electron-donating and electron-withdrawing substituents. Best results were seen with less basic anilines and highly activated acetanilides, reflecting the likelihood of different mechanistic pathways.

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