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2,5-dibromo-3,4-dimethylbenzoic acid is an organic compound characterized by its molecular formula C9H8Br2O2. 2,5-dibromo-3,4-dimethylbenzoic acid features a benzoic acid backbone, with two bromine atoms attached at the 2nd and 5th carbon positions, and two methyl groups at the 3rd and 4th carbon positions. The presence of bromine atoms imparts the molecule with significant halogenation, which can influence its chemical reactivity and physical properties. The dimethyl substitution on the benzene ring affects the electronic distribution and steric hindrance within the molecule. 2,5-dibromo-3,4-dimethylbenzoic acid is typically synthesized for use in the pharmaceutical and chemical industries, where it may serve as an intermediate in the synthesis of more complex molecules or as a reagent in various chemical reactions. Its specific applications can range from the production of dyes to the creation of pharmaceutical compounds, highlighting its versatility in organic chemistry.

6514-83-6

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6514-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6514-83-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,1 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6514-83:
(6*6)+(5*5)+(4*1)+(3*4)+(2*8)+(1*3)=96
96 % 10 = 6
So 6514-83-6 is a valid CAS Registry Number.

6514-83-6Upstream product

6514-83-6Relevant academic research and scientific papers

Compound as DMXAA-Pyranoxanthone well as preparation method and application thereof

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Paragraph 0041-0046, (2020/02/19)

The invention discloses a DMXAA-Pyranoxanthone heterozygous compound with an anti-tumor effect and a preparation method and application thereof. The DMXAA-Pyranoxanthone heterozygous compound adopts the structural formula shown as a formula I. The preparation method comprises the following steps: preparing DMXAA in three steps, preparing pyranoxanthone in two steps, and combining the DMXAA and the pyranoxanthone into the DMXAA-Pyranoxanthone heterozygous compound in two steps. The DMXAA-Pyranoxanthone heterozygous compound and a DMXAA/pyranoxanthone combined medicine have excellent in-vitro tumor cell proliferation inhibiting activity on breast cancer cells, liver cancer cells, leukemia cells, and can induce apoptosis of tumor cells through multiple targets. The DMXAA-Pyranoxanthone heterozygous compound and the DMXAA/pyranoxanthone combined medicine can be applied to preparation of cancer treating medicines.

A new short synthesis of 5,6-dimethylxanthenone-4-acetic acid (ASA404, DMXAA)

Yang, Shangjin,Denny, William A.

experimental part, p. 3945 - 3947 (2009/10/04)

A new short synthesis of 5,6-dimethylxanthenone-4-acetic acid (ASA404) is developed. The key steps of the synthesis are dibromination of 3,4-dimethylbenzoic acid, followed by regioselective coupling with 2-hydroxyphenylacetic acid and subsequent cyclodehydration.

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