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4,2'-dinitro-deoxybenzoin is a chemical compound with the molecular formula C14H8N2O6. It is a derivative of deoxybenzoin, which is a naturally occurring compound found in certain plants. The compound is characterized by the presence of two nitro groups (-NO2) at the 4th and 2nd positions of the benzene ring, respectively. This yellow crystalline solid is used as a reagent in organic synthesis, particularly for the detection of aldehydes and ketones. It is also employed in the preparation of other chemical compounds and has potential applications in the pharmaceutical and chemical industries. Due to its reactivity and potential hazards, it is important to handle 4,2'-dinitro-deoxybenzoin with care, following proper safety protocols.

3769-88-8

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3769-88-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3769-88-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,6 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3769-88:
(6*3)+(5*7)+(4*6)+(3*9)+(2*8)+(1*8)=128
128 % 10 = 8
So 3769-88-8 is a valid CAS Registry Number.

3769-88-8Downstream Products

3769-88-8Relevant academic research and scientific papers

Atroposelective Arene Formation by Carbene-Catalyzed Formal [4+2] Cycloaddition

Xu, Ke,Li, Wenchang,Zhu, Shaoheng,Zhu, Tingshun

, p. 17625 - 17630 (2019/11/29)

Atroposelective arene formation is an efficient method to build axially chiral molecules with multi-substituted arenes. Reported here is an organocatalyzed atroposelective arene formation reaction by an N-heterocyclic carbene (NHC) catalyzed formal [4+2] cycloaddition of conjugated dienals and α-aryl ketones. This study expands the synthetic potential of NHC organocatalysis and provides a competitive pathway for the synthesis of axially chiral ligands, catalysts, and other functional molecules.

Enamines: Part V - Synthesis of Substituted Phenyl Benzyl Ketones and 2-Arylisatogens

Kulkarni, Sheshgiri N.,Kamath, H. V.,Bhamare, N. K.

, p. 667 - 669 (2007/10/02)

Three different approaches of o/p-nitrophenyl benzyl ketones and their limitation in the synthesis of 2-arylisatogens are described.

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