4033-88-9 Usage
General Description
DIMETHYL 2-(4-NITROPHENYL)MALONATE is a chemical compound with the molecular formula C11H10N2O6. It is a yellow crystalline solid with a molecular weight of 258.20 g/mol. DIMETHYL 2-(4-NITROPHENYL)MALONATE is commonly used as a reagent in organic synthesis and pharmaceutical research. It is a malonate derivative with a nitrophenyl group attached to the second carbon atom of the malonate ester. DIMETHYL 2-(4-NITROPHENYL)MALONATE is known for its ability to undergo a variety of chemical reactions, including esterification, reduction, and hydrolysis, making it a versatile building block for the synthesis of other organic compounds. It is important to handle and store this compound with care, as it may pose health and environmental hazards if not managed properly.
Check Digit Verification of cas no
The CAS Registry Mumber 4033-88-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,3 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4033-88:
(6*4)+(5*0)+(4*3)+(3*3)+(2*8)+(1*8)=69
69 % 10 = 9
So 4033-88-9 is a valid CAS Registry Number.
4033-88-9Relevant articles and documents
SUBSTITUTED PYRAZOLYL-BASED CARBOXAMIDE AND UREA DERIVATIVES BEARING A PHENYL MOIETY SUBSTITUTED WITH AN O-CONTAINING GROUP AS VANILLOID RECEPTOR LIGANDS
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Page/Page column 141, (2013/05/23)
The invention relates to substituted pyrazolyl-based carboxamide and urea derivatives of formula (Q) as vanilloid receptor ligands, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.
Dimethyl malonate as a one-carbon source: A novel method of introducing carbon substituents onto aromatic nitro compounds
Selvakumar,Yadi Reddy,Sunil Kumar,Iqbal, Javed
, p. 8395 - 8398 (2007/10/03)
A number of carbon substituents possessing various functional groups could be introduced onto aromatic nitro compounds using dimethyl malonate as a one-carbon source and linker. Decarboxylation of both the ester groups originating from dimethyl malonate in this methodology is particularly significant.
