24000-79-1 Usage
Composition
1,4-Benzenedicarboxylic acid unit
1-Methyl ester group
4-[2-[4-(Methoxycarbonyl)benzoyl]hydrazide] moiety
Common Uses
Intermediate in the synthesis of pharmaceuticals and organic compounds
Manufacturing of polymers and plastics
Reactivity
May react with certain chemicals or under specific conditions
Flammability
Potentially flammable, depending on concentration and conditions
Irritability
May cause irritation upon contact with skin, eyes, or respiratory system
Safety Precautions
Handle with caution in laboratory and industrial settings
Follow proper safety protocols for handling, storage, and disposal
Health Hazards
Potential for skin, eye, and respiratory irritation
May cause other adverse health effects depending on exposure levels and duration
Environmental Hazards
Potential for environmental contamination if not handled and disposed of properly
May have negative effects on aquatic life and ecosystems
Regulatory Compliance
Be aware of any specific guidelines or restrictions related to the use and management of 1,4-Benzenedicarboxylicacid, 1-methyl ester, 4-[2-[4-(methoxycarbonyl)benzoyl]hydrazide]
Check Digit Verification of cas no
The CAS Registry Mumber 24000-79-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,0 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24000-79:
(7*2)+(6*4)+(5*0)+(4*0)+(3*0)+(2*7)+(1*9)=61
61 % 10 = 1
So 24000-79-1 is a valid CAS Registry Number.
24000-79-1Relevant academic research and scientific papers
Synthesis of α-aminocarbonyl compounds via hetero dielsalder reaction
Sakurai, Masayoshi,Kihara, Nobuhiro,Watanabe, Nobuhiro,Ikari, Yoshihiro,Takata, Toshikazu
supporting information, p. 144 - 147 (2018/01/01)
A synthetic route to α-aminoketone derivatives via a hetero DielsAlder reaction is described. Diacylhydrazine was oxidized by tert-butyl hypochlorite in the presence of pyridine. After evaporation, the hetero DielsAlder reaction with diene was carried out without isolation of the azodicarbonyl compound. Quantitative hetero DielsAlder reaction was possible with 1 equivalent of diene when Hf(OTf)4 or AgOTf was used as the catalyst. The NN bond of the product was cleaved by SmI2-reduction in the presence of tert-BuOH in THF. Further, ozonolysis of the C=C double bond afforded the α-aminoketone derivative in excellent yield.
Two polymorphic forms of 2,5-bis-(4-methoxycarbonylphenyl)-1,3,4-oxadiazole
Reck, Guenter,Orgzall, Ingo,Schulz, Burkhard,Dietzel, Birgit
, p. o634-o635 (2007/10/03)
The title compound [systematic name: dimethyl 4,4′-(1,3,4-oxadiazole-2,5-diyl)diphenylenedicarboxylate], C18H14N2O5, crystallizes under similar conditions in two different orthorhombic crystalline forms. In both
