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2-Hydroxyl氨基-6-nitrotoluene is an organic compound with the chemical formula C7H8N2O3. It is a derivative of toluene, featuring a nitro group at the 6th position and a hydroxyl amino group at the 2nd position. 2-HYDROXYLAMINO-6-NITROTOLUENE is known for its potential applications in the synthesis of various chemical products, including dyes and pharmaceuticals. Due to its reactivity, it is important to handle it with care, as it may pose health and environmental risks. The compound's properties, such as its solubility and stability, can be influenced by the presence of the nitro and hydroxyl amino groups, making it a subject of interest in chemical research and development.

5805-95-8

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5805-95-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5805-95-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,0 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5805-95:
(6*5)+(5*8)+(4*0)+(3*5)+(2*9)+(1*5)=108
108 % 10 = 8
So 5805-95-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O3/c1-5-6(8-10)3-2-4-7(5)9(11)12/h2-4,8,10H,1H3

5805-95-8SDS

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 N-(2-methyl-3-nitrophenyl)hydroxylamine

1.2 Other means of identification

Product number -
Other names 2-Hydroxylamino-6-nitrotoluene

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:5805-95-8 SDS

5805-95-8Relevant academic research and scientific papers

Preparation of Some Acetylated, Reduced and Oxidized Derivatives of 2,4-Diaminotoluene and 2,6-Dinitrotoluene

Mori, Masa-aki,Inoue, Masami,Nunozawa, Tetsuji,Miyahara, Tatsuro,Kozuka, Hiroshi

, p. 4859 - 4861 (2007/10/02)

4-Acetylamino-2-hydroxylaminotoluene (4AA2HAT) and 2-hydroxylamino-6-nitrotoluene (2HA6NT) were prepared from 4-acetylamino-2-nitrotoluene (4AA2NT) and 2,6-dinitrotoluene (2,6-DNT), respectively, by reduction with zinc dust and NH4Cl. 2,6-Dinitrobenzylalcohol (2,6-DNB) and 2,6-dinitrobenzoic acid (2,6-DNBA) were prepared from 2,6-dinitrobenzaldehyde (2,6-DNBAl) by reduction with NaBH4 and by oxidation with KMnO4, respectively. 2-Acetylamino-4-aminobenzoic acid (2AA4ABA) was prepared from 4-nitroanthranilic acid (4NAA) by acetylation followed by reduction with NaBH4 and Pd-C. 2,4-Diacetylaminobenzoic acid (2,4-DAABA) was prepared from 4NAA by reduction with NaBH4 and Pd-C followed by acetylation. 4-Acetylamino-2-aminobenzoic acid (4AA2ABA) was prepared from 4NAA by reduction and acetylation followed by chelation with Cu(AcO)2.Keywords- 4-acetylamino-2-hydroxylaminotoluene; 2-hydroxylamino-6-nitrotoluene; 2,6-dinitrobenzylalcohol; 2,6-dinitrobenzoic acid; 2-acetylamino-4-aminobenzoic acid; 4-acetylamino-2-aminobenzoic acid; 2,4-diacetylaminobenzoic acid; carcinogenicity; mutagenicity; preparation

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