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4-bromobicyclo[2.2.2]octane-1-carboxylic acid is a chemical compound with the molecular formula C9H13BrO2. It is a derivative of bicyclo[2.2.2]octane, a bicyclic hydrocarbon, with a carboxylic acid group (-COOH) attached to the first carbon atom and a bromine atom (Br) at the fourth carbon atom. 4-bromobicyclo[2.2.2]octane-1-carboxylic acid is characterized by its unique molecular structure, which consists of two six-membered rings fused together in a chair-like conformation. The presence of the bromine atom and carboxylic acid group imparts specific chemical properties and reactivity to the molecule, making it a potential candidate for various applications in organic synthesis, pharmaceuticals, and materials science.

1989-50-0

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1989-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1989-50-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,8 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1989-50:
(6*1)+(5*9)+(4*8)+(3*9)+(2*5)+(1*0)=120
120 % 10 = 0
So 1989-50-0 is a valid CAS Registry Number.

1989-50-0Downstream Products

1989-50-0Relevant academic research and scientific papers

HETEROBICYCLIC METALLOPROTEASE INHIBITORS

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Page/Page column 171-172, (2008/06/13)

The present invention relates generally to amide group containing pharmaceutical agents, and in particular, to amide containing heterobicyclic metalloprotease inhibitor compounds. More particularly, the present invention provides a new class of heterobicyclic MMP- 13 inhibiting compounds, that exhibit an increased potency in relation to currently known MMP- 13 inhibitors.

Polar Substituent Effects on 19F Chemical Shifts of Aryl and Vinyl Fluorides: A Fluorine-19 Nuclear Magnetic Resonance Study of Some 1,1-Difluoro-2-(4-substituted-bicyclooct-1-yl)ethenes

Adcock, William,Kok, Gaik B.

, p. 1079 - 1087 (2007/10/02)

An extensive series of 1,1-difluoro-2-(4-substituted-bicyclooct-1-yl)ethenes (2) covering a diverse range of substituents ( X = H, NO2, CN, CF3, COOCH3, F, Cl, Br, OCH3, C6H5, C2H, C2Si(CH3)3, CH3, and C(CH3)3) have been synthesized and their 19F N

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