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(R3a,R7a)-(1,3-dimethyl)-2-phenyl-2,3,3a,4,5,6,7,7a-octahydro-1H-1,3,2-benzodiazaphosphole 2-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

184535-50-0

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184535-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 184535-50-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,5,3 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 184535-50:
(8*1)+(7*8)+(6*4)+(5*5)+(4*3)+(3*5)+(2*5)+(1*0)=150
150 % 10 = 0
So 184535-50-0 is a valid CAS Registry Number.

184535-50-0Relevant academic research and scientific papers

An efficient method for the synthesis of N,N′-dimethyl-1,2-diamines

Tye, Heather,Eldred, Colin,Wills, Martin

, p. 155 - 158 (2007/10/03)

A simple method for the preparation of N,N′-dimethyl-1,2-diamines is described. The method requires the dimethylation of a diazaphospholidine oxide followed by acid-catalysed hydrolysis.

The asymmetric synthesis of α-substituted α-methyl and α-phenyl phosphonic acids: Design, carbanion geometry, reactivity and preparative aspects of chiral alkyl bicyclic phosphonamides

Bennani, Youssef L.,Hanessian, Stephen

, p. 13837 - 13866 (2007/10/03)

The design, preparation, structural and spectroscopic analyses of topologically unique and enantiomerically pure alkyl phosphonamides are described. In the case of α-ethyl and α-benzyl phosphonamides, the geometry of both the secondary and tertiary carbanions was determined to be planar through deprotonation/deuteration/alkylation experiments. Stereoselective alkylations of such systems proceeded in good yields and with high diastereoselectivities. The resulting α,α-alkylated phosphonamides were hydrolyzed to give the corresponding α,α-alkyl phosphonic acids with high degrees of enantiomeric purity.

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