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1H-Indole-3-carboxylic acid, 2-(bromomethyl)-1-(phenylsulfonyl)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

154953-45-4

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154953-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154953-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,9,5 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 154953-45:
(8*1)+(7*5)+(6*4)+(5*9)+(4*5)+(3*3)+(2*4)+(1*5)=154
154 % 10 = 4
So 154953-45-4 is a valid CAS Registry Number.

154953-45-4Downstream Products

154953-45-4Relevant academic research and scientific papers

Unusual dimerization of N-protected bromomethylindoles using phenylmagnesium chloride

Mohanakrishnan, Arasambattu K.,Ramesh, Neelamegam,Prakash, Chandran

, p. 6983 - 6985 (2005)

A novel dimerization of N-protected bromomethylindoles involving an exchange reaction with phenylmagnesium chloride is reported.

Synthesis of N-protected indolaldehydes using modified Hass procedure

Balamurugan, Ramalingam,Mohanakrishnan, Arasambattu K.

, p. 11078 - 11085 (2008/02/12)

A detailed study on oxidation of N-protected bromomethylindoles into the respective aldehydes was carried out. Using a modified Hass procedure, synthesis of aryl-/hetero-aryl aldehydes in particular indolaldehydes is achieved in reasonable yields.

A facile preparation of N-protected indolaldehydes using a modified Hass procedure

Mohanakrishnan, Arasambattu K.,Balamurugan, Ramalingam,Ramesh, Neelamegam

, p. 8189 - 8193 (2007/10/03)

The preparation of a variety of N-protected indolaldehydes is reported via the reaction of N-protected bromomethylindoles with 2-nitropropane using NaH/DMF.

An efficient preparation of 1-phenylsulfonylindolyl methyl sulfoxides using KF/m-CPBA

Mohanakrishnan, Arasambattu K.,Ramesh, Neelamegam

, p. 4231 - 4233 (2007/10/03)

A variety of 1-phenylsulfonylindolylmethyl sulfides are selectively oxidized to the corresponding sulfoxides using a hitherto unexplored KF/m-CPBA system. A major advantage is the absence of over-oxidation.

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