96839-34-8 Usage
Appearance
Pale yellow solid 2,6-dinitrobenzyl alcohol has a pale yellow color and is a solid at room temperature.
Odor
Slightly sweet The compound has a mild, sweet odor that can be detected.
Primary use
Cross-linking agent in polymer and resin manufacturing 2,6-dinitrobenzyl alcohol is mainly used to connect and strengthen polymer and resin structures.
Secondary use
Reagent in organic synthesis The compound is also utilized as a reagent in the formation of esters and ethers in organic chemistry.
Potential applications
Photolithography and photoprotecting group 2,6-dinitrobenzyl alcohol has been researched for its possible applications in photolithography processes and as a protective group in organic chemistry.
Toxicity
Handle with care 2,6-dinitrobenzyl alcohol is toxic, and proper safety precautions should be taken when handling it.
Skin and eye irritation
Can cause irritation The compound may cause skin and eye irritation upon contact.
Ingestion and inhalation hazards
May be harmful Ingesting or inhaling 2,6-dinitrobenzyl alcohol can lead to harmful health effects.
Check Digit Verification of cas no
The CAS Registry Mumber 96839-34-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,8,3 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96839-34:
(7*9)+(6*6)+(5*8)+(4*3)+(3*9)+(2*3)+(1*4)=188
188 % 10 = 8
So 96839-34-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O5/c10-4-5-6(8(11)12)2-1-3-7(5)9(13)14/h1-3,10H,4H2
96839-34-8Relevant 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
