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1-bromo-3-chloro-2,5-dimethoxy-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

252044-83-0

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252044-83-0 Usage

Benzene derivative

Yes

Explanation

1-bromo-3-chloro-2,5-dimethoxy-benzene is derived from benzene, a basic aromatic compound consisting of a six-carbon ring with alternating single and double bonds.

Explanation

The compound contains one bromine and one chlorine atom, which are both halogens. These atoms contribute to the compound's reactivity and properties.

Explanation

The compound has two methoxy (CH3O) groups attached to the benzene ring, which are derived from methanol (CH3OH).

Explanation

The bromine atom is attached to the first carbon of the benzene ring, the chlorine atom to the third carbon, and the two methoxy groups are attached to the second and fifth carbons.

Explanation

1-bromo-3-chloro-2,5-dimethoxy-benzene is often used as a starting material in the synthesis of more complex organic molecules due to its unique structure and reactivity.

Explanation

The compound's versatility in chemical reactions makes it valuable in the development of various products, including pharmaceuticals, agrochemicals, and materials for scientific research and applications.

Explanation

Both bromine and chlorine are toxic and can pose health risks if not properly managed. Care should be taken when handling 1-bromo-3-chloro-2,5-dimethoxy-benzene to minimize exposure and ensure safety.

Explanation

Due to the potential toxicity of bromine and chlorine, it is important to handle 1-bromo-3-chloro-2,5-dimethoxy-benzene with care, using appropriate safety measures and equipment.

Halogen atoms

Bromine (Br) and Chlorine (Cl)

Methoxy groups

Two (2)

Position of functional groups

1-bromo, 3-chloro, 2,5-dimethoxy

Use in organic synthesis

Building block

Applications

Pharmaceuticals, agrochemicals, and materials science

Toxicity

Potential health risks due to bromine and chlorine

Handling precautions

Careful handling required

Check Digit Verification of cas no

The CAS Registry Mumber 252044-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,0,4 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 252044-83:
(8*2)+(7*5)+(6*2)+(5*0)+(4*4)+(3*4)+(2*8)+(1*3)=110
110 % 10 = 0
So 252044-83-0 is a valid CAS Registry Number.

252044-83-0Relevant academic research and scientific papers

OXOACRIDINYL ACETIC ACID DERIVATIVES AND METHODS OF USE

-

, (2019/06/05)

Compounds of Formula I or pharmaceutically acceptable salts or esters thereof capable of binding to and modulating the activity of a stimulator of interferon genes (STING) protein are provided. Methods involving compounds of Formula I as effective modulators of STING are also provided.

A concise total synthesis of (±)-A80915G, a member of the napyradiomycin family of antibiotics

Takemura, Shunji,Hirayama, Aya,Tokunaga, Junko,Kawamura, Fumie,Inagaki, Kyoko,Hashimoto, Kimiko,Nakata, Masaya

, p. 7501 - 7505 (2007/10/03)

(±)-A80915G, a member of the napyradiomycin family of antibiotics, has been synthesized from 1-amino-2,5-dimethoxy-4-nitrobenzene via the sequential palladium-catalyzed cross-coupling reactions (the Stille reaction) of aryl halides with allyltins and the Diels-Alder reaction of the chloroquinone with the Danishefsky-Brassard diene.

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