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2-(2,6-Dibromo-4-methylphenoxy)ethyl Bromide is a chemical compound with the molecular formula C9H10Br3O. It is a brominated derivative of phenol, characterized by the presence of two bromine atoms at the 2nd and 6th positions of the phenyl ring, and a methyl group at the 4th position. The compound is also known as 2-(2,6-dibromo-4-methylphenoxy)ethyl bromide or 2-(2,6-dibromo-4-methylphenyl)ethyl bromide. It is a colorless to pale yellow liquid with a density of 1.84 g/cm3 and a melting point of 21-23°C. 2-(2,6-Dibromo-4-methylphenoxy)ethyl Bromide is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its reactive bromine atoms and phenolic structure. It is important to handle 2-(2,6-Dibromo-4-methylphenoxy)ethyl Bromide with care, as it is toxic and can cause harm to the environment and human health.

76429-67-9

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76429-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76429-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,2 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76429-67:
(7*7)+(6*6)+(5*4)+(4*2)+(3*9)+(2*6)+(1*7)=159
159 % 10 = 9
So 76429-67-9 is a valid CAS Registry Number.

76429-67-9Relevant academic research and scientific papers

CARBOXAMIDES USEFUL AS ANTIEMETIC OR ANTIPSYCHOTIC AGENTS

-

, (2008/06/13)

Carboxamides represented by the formula (I): STR1 wherein Z represents the carbon atoms necessary to complete a 5-to 7-membered ring, R 1, R 2, and R 3 may be the same or different and are selected from the group consisting of a hydrogen atom, a lower alkyl group, a cycloalkyl group, a halogen atom, an amino group, a lower alkylamino group, an alkoxy group, an acylamido group, a sulfonamido group, and a nitro group; andA represents an aminoalkyl moiety and acid addition salts thereof.

Oxygen Heterocycles by the Parham Cyclialkylation

Bradsher, Charles K.,Reames, David C.

, p. 1384 - 1388 (2007/10/02)

The addition of butyllithium at -100 deg C to ω-bromoalkyl ethers of o-bromophenol (and its congeners) led to preferential exchange of the aryl bromine at position 2.The resulting organolithium reagents, under suitable conditions, cyclized to afford 2,3-dihydrobenzofurans (6), 3,4-dihydro-2H-1-benzopyrans (13), or 2,3,4,5-tetrahydro-1-benzoxepins (16) in good yields, but less satisfactory results were obtained with the intermediate expected to produce 8-methyl-3,4,5,6-tetrahydro-2H-1-benzoxocin (19). ω-Bromoethyl and ω-bromopropyl ethers of suitable dibromophenols were treated successively with 2 equiv of butyllithium and an electrophile to yield derivatives of 6 and 13.

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