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Benzaldehyde, 2-bromo-4,5-bis(phenylmethoxy)-, is an organic compound with the chemical formula C20H17BrO2. It is a derivative of benzaldehyde, featuring a bromine atom at the 2-position and two phenylmethoxy groups attached to the 4 and 5 positions of the benzene ring. Benzaldehyde, 2-bromo-4,5-bis(phenylmethoxy)- is characterized by its molecular weight of 371.25 g/mol and a melting point of 76-78°C. It is a colorless to pale yellow crystalline solid and is soluble in organic solvents such as ethanol and dichloromethane. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity.

4816-00-6

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4816-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4816-00-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,1 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4816-00:
(6*4)+(5*8)+(4*1)+(3*6)+(2*0)+(1*0)=86
86 % 10 = 6
So 4816-00-6 is a valid CAS Registry Number.

4816-00-6Relevant academic research and scientific papers

Total synthesis of altenusin and alterlactone

Cudaj, Judith,Podlech, Joachim

supporting information; experimental part, p. 371 - 374 (2012/03/27)

The resorcylic lactone alterlactone, a mycotoxin produced by alternaria sp., was synthesized for the first time. The total synthesis was achieved in nine steps with 69% yield starting with acetal-protected phloroglucinic acid and 6-bromopiperonal, where t

A concise benzotriazolyl-mediated synthesis of 9-methoxycepharanone A

Rys, Véronique,Couture, Axel,Deniau, Eric,Lebrun, Stéphane,Grandclaudon, Pierre

, p. 665 - 671 (2007/10/03)

A concise synthesis of 9-methoxycepharanone A is described. The key step is the benzotriazolyl-assisted assemblage of an arylmethyleneisoindolinone ring system comprising the enol ether unit. Radical cyclization followed by deprotections and ultimate formation of the methylenedioxy group complete the total synthesis of the title compound. Graphical Abstract.

Studies on Mannich Reaction of 1-Benzyltetrahydroisoquinolines

Bhakuni, D. S.,Kumar, Praveen

, p. 417 - 421 (2007/10/02)

The effect of substituents in Mannich cyclisation reaction of 1-benzyltetrahydroisoquinolines has been studied.Both para- and ortho-cyclisation products are formed when hydroxyl groups are present in the benzene ring of the benzylic moiety whereas only pa

Synthesis of Ring-Alkylated Isoproterenol Derivatives

Reitz, Allen,Avery, Mitchell A.,Verlander, Michael S.,Goodman, Murray

, p. 4859 - 4863 (2007/10/02)

2-Propyl-, 5-propyl-, and 6-propylisoproterenols (2a, 2b, and 1d, respectively) have been synthesized as models for polymer drug conjugates.Key intermediates were the propenylbenzaldehydes 3a-c.The (isopropylamino)phenethanol side chain was constructed fr

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