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78283-22-4

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78283-22-4 Usage

General Description

2,6-Dinitrophenyl acetaldehyde is a chemical compound with the molecular formula C8H6N2O7. It is an organic compound that is commonly used in organic synthesis and chemical research. It is a yellow solid with a distinctive odor and is highly explosive under certain conditions. 2,6-Dinitrophenyl acetaldehyde is used as a reagent in the preparation of various organic compounds and as a starting material for the synthesis of other chemicals. It is also known for its use in the detection and analysis of aldehydes and ketones through the formation of colored derivatives. Due to its explosive nature and potential health hazards, it should be handled and stored with caution, following proper safety protocols.

Check Digit Verification of cas no

The CAS Registry Mumber 78283-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,2,8 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78283-22:
(7*7)+(6*8)+(5*2)+(4*8)+(3*3)+(2*2)+(1*2)=154
154 % 10 = 4
So 78283-22-4 is a valid CAS Registry Number.

78283-22-4SDS

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 (2,6-Dinitrophenyl)acetaldehyde

1.2 Other means of identification

Product number -
Other names 2,6-Dinitro-p-cresol

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:78283-22-4 SDS

78283-22-4Relevant articles and documents

Synthetic Studies in the Indole Series. Preparation of the Unique Antibiotic Alkaloid Chuangxinmycin by a Nitro Group Displacement Reaction

Kozikowski, Alan P.,Greco, Michael N.,Springer, James P.

, p. 7622 - 7626 (2007/10/02)

The total synthesis of the unique sulfur-containing antibiotic indole alkaloid chuangxinmycin is described.This compound, first isolated by Chinese chemists at the Institute of Materia Medica, was assembled from 2,6-dinitrotoluene by a scheme that combine

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