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200295-57-4

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200295-57-4 Usage

General Description

4-Nitro-1,3-phenylenediamine sulfate is a chemical compound that is commonly used as a hair dye and in the manufacturing of other dye products. It is a synthetic organic compound that is a derivative of phenylenediamine and contains a nitro group. The sulfate salt form of this compound is water-soluble and is commonly used in hair dye formulations to produce shades of brown and black. Due to its potential to cause allergic reactions and skin irritation, its use in hair dye products is heavily regulated, and it is often labeled as a potential allergen. Additionally, 4-Nitro-1,3-phenylenediamine sulfate is also used in the preparation of other dye products for textiles and plastics.

Check Digit Verification of cas no

The CAS Registry Mumber 200295-57-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,2,9 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 200295-57:
(8*2)+(7*0)+(6*0)+(5*2)+(4*9)+(3*5)+(2*5)+(1*7)=94
94 % 10 = 4
So 200295-57-4 is a valid CAS Registry Number.

200295-57-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitrobenzene-1,3-diamine,sulfuric acid

1.2 Other means of identification

Product number -
Other names UNII-S9D878Z314

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:200295-57-4 SDS

200295-57-4Downstream Products

200295-57-4Relevant articles and documents

Silver-Catalyzed Three-Component Coupling Reaction of Amines, 2-Isocyanobenzaldehydes, and 2,2,2-Trifluorodiazoethane and Synthesis of Trifluoromethyl-Substituted Indolo[1,2-c]quinazolines

Meng, Xiang-He,Peng, Ju-Yin,Yang, Ming,Zhao, Yu-Long

supporting information, p. 244 - 250 (2020/12/01)

A silver-catalyzed three-component coupling reaction of amines, 2-isocyanobenzaldehydes, and 2,2,2-trifluorodiazoethane has been developed. This reaction provides an efficient method for the construction of CF3-containing dihydroquinazolines. On the basis of this reaction, using trifluorodiazoethyl-substituted dihydroquinazolines as synthons, trifluoromethyl-substituted indolo[1,2-c]quinazolines were prepared in high yields via a TBHP/KI-mediated sequential intramolecular cyclization and aromatization process. (Figure presented.).

Repurposing an Aldolase for the Chemoenzymatic Synthesis of Substituted Quinolines

Fansher, Douglas J.,Granger, Richard,Kaur, Satinderpal,Palmer, David R. J.

, p. 6939 - 6943 (2021/06/28)

Quinoline derivatives are important natural products and pharmaceuticals, but their synthesis can be challenging due to poor yields, harsh reaction conditions, and instability of starting materials. Here we report the chemoenzymatic synthesis of quinaldic acids under mild conditions using an aldolase, trans-o-hydroxybenzylidenepyruvate hydratase-aldolase (NahE, or HBPA). A series of 2-aminobenzaldehydes derived from reduction of the corresponding nitro analogue were reacted with pyruvate in the presence of NahE to give substituted quinolines in up to 93% isolated yield. This reaction differs from the aldol condensation catalyzed by NahE in vivo, instead resembling the heterocycle formation catalyzed by its homologue, dihydrodipicolinate synthase.

ALDEHYDE CONJUGATES AND USES THEREOF

-

Paragraph 0306; 0315-0316, (2020/08/20)

The present invention provides compounds and methods of use thereof for the treatment, prevention, and/or reduction of a risk of a disease, disorder, or condition in which aldehyde toxicity is implicated in the pathogenesis, including ocular disorders, skin disorders, conditions associated with injurious effects from blister agents, and autoimmune, inflammatory, neurological and cardiovascular diseases by the use of a primary amine to scavenge toxic aldehydes, such as MDA and HNE.

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