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2-Dideuterioaminobromobenzene is an organic compound with the molecular formula C6H5BrND2. It is a derivative of aminobromobenzene, where two hydrogen atoms are replaced by deuterium atoms. Deuterium is a stable isotope of hydrogen, which makes 2-dideuterioaminobromobenzene useful in various applications, such as in chemical reactions and spectroscopic studies. The presence of the bromine atom and the deuterated amino group in the molecule can affect its reactivity, stability, and physical properties compared to its non-deuterated counterpart. 2-dideuterioaminobromobenzene can be synthesized through various chemical reactions and is often used as a building block in the synthesis of more complex organic molecules or as a reagent in organic chemistry research.

2987-42-0

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2987-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2987-42-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,8 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2987-42:
(6*2)+(5*9)+(4*8)+(3*7)+(2*4)+(1*2)=120
120 % 10 = 0
So 2987-42-0 is a valid CAS Registry Number.

2987-42-0Upstream product

2987-42-0Relevant academic research and scientific papers

Copper-catalyzed ortho-halogenation of protected anilines

Urones, Beatriz,Martinez, Angel Manu,Rodriguez, Nuria,Arrayas, Ramon Gomez,Carretero, Juan C.

, p. 11044 - 11046 (2013)

A practical Cu-catalyzed direct ortho-halogenation of anilines under aerobic conditions has been developed. The reaction shows typically excellent mono-substitution selectivity, high ortho-regiocontrol and large functional group tolerance.

Palladium-catalyzed oxidative cyclization of N-aryl enamines: From anilines to indoles

Wuertz, Sebastian,Rakshit, Souvik,Neumann, Julia J.,Droege, Thomas,Glorius, Frank

supporting information; experimental part, p. 7230 - 7233 (2009/04/10)

(Chemical Equation Presented) The special advantage of the title reaction to form substituted indoles 2 lies within the broad scope of the transformation: A multitude of N-aryl enaminones 1 can be prepared readily in one step from commercially available anilines. Furthermore, anilines can be converted directly in a one-pot process into the indole products. R1 = H, Me, OMe, Cl, F, carbonyl functionality, CN, fused aryl; R2 = alkyl, aryl; R 3 = alkyl, O-alkyl.

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